Carbon (Carbon Activated)

别名: 碳;活性碳;活性炭粉;活性炭颗粒;活性炭[用分子氧做氧化反应的催化剂];Charcoal Activated [Catalyst for Oxidation using Molecular Oxygen] 活性炭[用分子氧做氧化反应的催化剂]
目录号: V66389 纯度: ≥98%
碳可用作药物赋形剂,例如脱色剂。
Carbon (Carbon Activated) CAS号: 7440-44-0
产品类别: Biochemical Assay Reagents
产品仅用于科学研究,不针对患者销售
规格 价格
500mg
1g
Other Sizes

Other Forms of Carbon (Carbon Activated):

  • Carbon-13C (Multi-walled carbon nanotubes (industrial grade)-13C)
点击了解更多
InvivoChem产品被CNS等顶刊论文引用
产品描述
碳可用作药物赋形剂,例如脱色剂。药用辅料或药用助剂是指制药过程中使用的除药物成分以外的其他化学物质。药用辅料一般是指药物制剂中的非活性成分,能提高药物制剂的稳定性、溶解度和加工性能。药用辅料还会影响并用药物的吸收、分布、代谢和消除 (ADME) 过程。
生物活性&实验参考方法
药代性质 (ADME/PK)
吸收、分布和排泄
实验表明,向兔子静脉注射纯碳悬浮液不会引起眼部炎症,尽管碳颗粒沉积在血管内。
毒性/毒理 (Toxicokinetics/TK)
非人类毒性值
大鼠口服LD50 > 10,000 mg/kg
小鼠静脉注射LD50 440 mg/kg
参考文献

[1]. Pharmaceutical excipients - quality, regulatory and biopharmaceutical considerations. Eur J Pharm Sci. 2016 May 25;87:88-99.

其他信息
根据世界卫生组织国际癌症研究机构 (IARC) 的说法,炭黑(空气中可吸入的游离颗粒)可能致癌。
活性炭是一种经过处理以提高吸附能力的黑色颗粒。如果在生产后未适当冷却,可能会自燃。
动物或植物来源的碳呈黑色粉末或颗粒状,与焦油或淀粉和水粘合剂混合,压制成规则的块状或煤球状。加热缓慢,在空气中易燃,尤其是在潮湿的情况下。
碳纳米管是由石墨烯圆柱体组成的富勒烯状纳米结构。其末端由五边形环封闭。
碳是一种非金属四价元素,符号为C,原子序数为6,原子量为12。
碳是一种矿物。
另见:炭黑(有子类);石墨(有子类)。活性炭(有子类)……查看更多……
*注: 文献方法仅供参考, InvivoChem并未独立验证这些方法的准确性
化学信息 & 存储运输条件
分子式
C
精确质量
12
CAS号
7440-44-0
相关CAS号
Carbon-13C;14762-74-4
PubChem CID
5462310
外观&性状
Steel gray to black greasy feeling solid.
密度
~1.7 g/mL at 25 °C(lit.)
沸点
500-600 °C(lit.)
熔点
Melting point equals greater than 3500 °C ; MW: 760.642 Yellow needles of plates. MP: >280 °C. Soluble in organic solvents /Fullerene-60/ ; MW: 840.749. Red-brown solid. MP: >280 °C. Soluble in benzene, toluene /Fullerene-70/ ; >3500 °C ; 4489 °C ; 6602 °F (Sublimes)
闪点
>230 °F
蒸汽压
<0.1 mm Hg ( 20 °C)
LogP
0.6
tPSA
0
氢键供体(HBD)数目
0
氢键受体(HBA)数目
0
可旋转键数目(RBC)
0
重原子数目
1
分子复杂度/Complexity
0
定义原子立体中心数目
0
SMILES
[C]
InChi Key
OKTJSMMVPCPJKN-UHFFFAOYSA-N
InChi Code
InChI=1S/C
化学名
carbon
HS Tariff Code
2934.99.9001
存储方式

Powder      -20°C    3 years

                     4°C     2 years

In solvent   -80°C    6 months

                  -20°C    1 month

运输条件
Room temperature (This product is stable at ambient temperature for a few days during ordinary shipping and time spent in Customs)
溶解度数据
溶解度 (体外实验)
May dissolve in DMSO (in most cases), if not, try other solvents such as H2O, Ethanol, or DMF with a minute amount of products to avoid loss of samples
溶解度 (体内实验)
注意: 如下所列的是一些常用的体内动物实验溶解配方,主要用于溶解难溶或不溶于水的产品(水溶度<1 mg/mL)。 建议您先取少量样品进行尝试,如该配方可行,再根据实验需求增加样品量。

注射用配方
(IP/IV/IM/SC等)
注射用配方1: DMSO : Tween 80: Saline = 10 : 5 : 85 (如: 100 μL DMSO 50 μL Tween 80 850 μL Saline)
*生理盐水/Saline的制备:将0.9g氯化钠/NaCl溶解在100 mL ddH ₂ O中,得到澄清溶液。
注射用配方 2: DMSO : PEG300Tween 80 : Saline = 10 : 40 : 5 : 45 (如: 100 μL DMSO 400 μL PEG300 50 μL Tween 80 450 μL Saline)
注射用配方 3: DMSO : Corn oil = 10 : 90 (如: 100 μL DMSO 900 μL Corn oil)
示例: 注射用配方 3 (DMSO : Corn oil = 10 : 90) 为例说明, 如果要配制 1 mL 2.5 mg/mL的工作液, 您可以取 100 μL 25 mg/mL 澄清的 DMSO 储备液,加到 900 μL Corn oil/玉米油中, 混合均匀。
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注射用配方 4: DMSO : 20% SBE-β-CD in Saline = 10 : 90 [如:100 μL DMSO 900 μL (20% SBE-β-CD in Saline)]
*20% SBE-β-CD in Saline的制备(4°C,储存1周):将2g SBE-β-CD (磺丁基-β-环糊精) 溶解于10mL生理盐水中,得到澄清溶液。
注射用配方 5: 2-Hydroxypropyl-β-cyclodextrin : Saline = 50 : 50 (如: 500 μL 2-Hydroxypropyl-β-cyclodextrin (羟丙基环胡精) 500 μL Saline)
注射用配方 6: DMSO : PEG300 : Castor oil : Saline = 5 : 10 : 20 : 65 (如: 50 μL DMSO 100 μL PEG300 200 μL Castor oil 650 μL Saline)
注射用配方 7: Ethanol : Cremophor : Saline = 10: 10 : 80 (如: 100 μL Ethanol 100 μL Cremophor 800 μL Saline)
注射用配方 8: 溶解于Cremophor/Ethanol (50 : 50), 然后用生理盐水稀释。
注射用配方 9: EtOH : Corn oil = 10 : 90 (如: 100 μL EtOH 900 μL Corn oil)
注射用配方 10: EtOH : PEG300Tween 80 : Saline = 10 : 40 : 5 : 45 (如: 100 μL EtOH 400 μL PEG300 50 μL Tween 80 450 μL Saline)


口服配方
口服配方 1: 悬浮于0.5% CMC Na (羧甲基纤维素钠)
口服配方 2: 悬浮于0.5% Carboxymethyl cellulose (羧甲基纤维素)
示例: 口服配方 1 (悬浮于 0.5% CMC Na)为例说明, 如果要配制 100 mL 2.5 mg/mL 的工作液, 您可以先取0.5g CMC Na并将其溶解于100mL ddH2O中,得到0.5%CMC-Na澄清溶液;然后将250 mg待测化合物加到100 mL前述 0.5%CMC Na溶液中,得到悬浮液。
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口服配方 3: 溶解于 PEG400 (聚乙二醇400)
口服配方 4: 悬浮于0.2% Carboxymethyl cellulose (羧甲基纤维素)
口服配方 5: 溶解于0.25% Tween 80 and 0.5% Carboxymethyl cellulose (羧甲基纤维素)
口服配方 6: 做成粉末与食物混合


注意: 以上为较为常见方法,仅供参考, InvivoChem并未独立验证这些配方的准确性。具体溶剂的选择首先应参照文献已报道溶解方法、配方或剂型,对于某些尚未有文献报道溶解方法的化合物,需通过前期实验来确定(建议先取少量样品进行尝试),包括产品的溶解情况、梯度设置、动物的耐受性等。

请根据您的实验动物和给药方式选择适当的溶解配方/方案:
1、请先配制澄清的储备液(如:用DMSO配置50 或 100 mg/mL母液(储备液));
2、取适量母液,按从左到右的顺序依次添加助溶剂,澄清后再加入下一助溶剂。以 下列配方为例说明 (注意此配方只用于说明,并不一定代表此产品 的实际溶解配方):
10% DMSO → 40% PEG300 → 5% Tween-80 → 45% ddH2O (或 saline);
假设最终工作液的体积为 1 mL, 浓度为5 mg/mL: 取 100 μL 50 mg/mL 的澄清 DMSO 储备液加到 400 μL PEG300 中,混合均匀/澄清;向上述体系中加入50 μL Tween-80,混合均匀/澄清;然后继续加入450 μL ddH2O (或 saline)定容至 1 mL;

3、溶剂前显示的百分比是指该溶剂在最终溶液/工作液中的体积所占比例;
4、 如产品在配制过程中出现沉淀/析出,可通过加热(≤50℃)或超声的方式助溶;
5、为保证最佳实验结果,工作液请现配现用!
6、如不确定怎么将母液配置成体内动物实验的工作液,请查看说明书或联系我们;
7、 以上所有助溶剂都可在 Invivochem.cn网站购买。
计算器

摩尔浓度计算器可计算特定溶液所需的质量、体积/浓度,具体如下:

  • 计算制备已知体积和浓度的溶液所需的化合物的质量
  • 计算将已知质量的化合物溶解到所需浓度所需的溶液体积
  • 计算特定体积中已知质量的化合物产生的溶液的浓度
使用摩尔浓度计算器计算摩尔浓度的示例如下所示:
假如化合物的分子量为350.26 g/mol,在5mL DMSO中制备10mM储备液所需的化合物的质量是多少?
  • 在分子量(MW)框中输入350.26
  • 在“浓度”框中输入10,然后选择正确的单位(mM)
  • 在“体积”框中输入5,然后选择正确的单位(mL)
  • 单击“计算”按钮
  • 答案17.513 mg出现在“质量”框中。以类似的方式,您可以计算体积和浓度。

稀释计算器可计算如何稀释已知浓度的储备液。例如,可以输入C1、C2和V2来计算V1,具体如下:

制备25毫升25μM溶液需要多少体积的10 mM储备溶液?
使用方程式C1V1=C2V2,其中C1=10mM,C2=25μM,V2=25 ml,V1未知:
  • 在C1框中输入10,然后选择正确的单位(mM)
  • 在C2框中输入25,然后选择正确的单位(μM)
  • 在V2框中输入25,然后选择正确的单位(mL)
  • 单击“计算”按钮
  • 答案62.5μL(0.1 ml)出现在V1框中
g/mol

分子量计算器可计算化合物的分子量 (摩尔质量)和元素组成,具体如下:

注:化学分子式大小写敏感:C12H18N3O4  c12h18n3o4
计算化合物摩尔质量(分子量)的说明:
  • 要计算化合物的分子量 (摩尔质量),请输入化学/分子式,然后单击“计算”按钮。
分子质量、分子量、摩尔质量和摩尔量的定义:
  • 分子质量(或分子量)是一种物质的一个分子的质量,用统一的原子质量单位(u)表示。(1u等于碳-12中一个原子质量的1/12)
  • 摩尔质量(摩尔重量)是一摩尔物质的质量,以g/mol表示。
/

配液计算器可计算将特定质量的产品配成特定浓度所需的溶剂体积 (配液体积)

  • 输入试剂的质量、所需的配液浓度以及正确的单位
  • 单击“计算”按钮
  • 答案显示在体积框中
动物体内实验配方计算器(澄清溶液)
第一步:请输入基本实验信息(考虑到实验过程中的损耗,建议多配一只动物的药量)
第二步:请输入动物体内配方组成(配方适用于不溶/难溶于水的化合物),不同的产品和批次配方组成不同,如对配方有疑问,可先联系我们提供正确的体内实验配方。此外,请注意这只是一个配方计算器,而不是特定产品的确切配方。
+
+
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计算结果:

工作液浓度 mg/mL;

DMSO母液配制方法 mg 药物溶于 μL DMSO溶液(母液浓度 mg/mL)。如该浓度超过该批次药物DMSO溶解度,请首先与我们联系。

体内配方配制方法μL DMSO母液,加入 μL PEG300,混匀澄清后加入μL Tween 80,混匀澄清后加入 μL ddH2O,混匀澄清。

(1) 请确保溶液澄清之后,再加入下一种溶剂 (助溶剂) 。可利用涡旋、超声或水浴加热等方法助溶;
            (2) 一定要按顺序加入溶剂 (助溶剂) 。

临床试验信息
Title:Ketamine, SGB and Combination Treatment for TBI-associated Headache or PTSD
Status:Recruiting
updateDate:2026-05-01
Ctid:NCT06608277

Link: https://clinicaltrials.gov/ct2/show/NCT06608277

Conditions:Posttraumatic Headache|Posttraumatic Stress Disorder
Interventions:Group C Experimental
Phase:Phase 2
Title:Vemurafenib Neoadjuvant Trial in Locally Advanced Thyroid Cancer
Status:Active, not recruiting
updateDate:2026-04-16
Ctid:NCT01709292

Link: https://clinicaltrials.gov/ct2/show/NCT01709292

Conditions:Thyroid Cancer
Interventions:Vemurafenib (Post Surgery) - Group A + C
Phase:Phase 2
Title:Efficacy and Safety Studies of Frexalimab (SAR441344) in Adults With Relapsing Forms of Multiple Sclerosis
Status:Recruiting
updateDate:2026-04-13
Ctid:NCT06141473

Link: https://clinicaltrials.gov/ct2/show/NCT06141473

Conditions:Multiple Sclerosis
Interventions:Activated charcoal
Phase:Phase 3
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Title:Measuring Acute Drug Demand in Humans
Status:Suspended
updateDate:2026-02-18
Ctid:NCT05829655

Link: https://clinicaltrials.gov/ct2/show/NCT05829655

Conditions:Opioid Use Disorder|Opioid Dependence
Interventions:Placebo
Phase:Early Phase 1
Title:Activated CHARcoal in Poisoned Patient - Pilot Trial
Status:Recruiting
updateDate:2026-01-29
Ctid:NCT05471479

Link: https://clinicaltrials.gov/ct2/show/NCT05471479

Conditions:Charcoal, Decontamination, Poisoning
Interventions:Activated Charcoal
Phase:Phase 4
Title:Perineural Dexamethasone, Dexmedetomidine, or Their Combination to Reduces Rebound Pain After Supraclavicular Brachial Plexus Block
Status:Not yet recruiting
updateDate:2026-01-09
Ctid:NCT07299877

Link: https://clinicaltrials.gov/ct2/show/NCT07299877

Conditions:Brachial Plexus Blocks
Interventions:Group C (Dexamethasone + Dexmedetomidine)
Phase:Phase 4
Title:Effect of Activated Charcoal on Serum Osmolality, Osmolal Gap, and Enzymatic Ethylene Glycol Assay
Status:Not yet recruiting
updateDate:2025-10-23
Ctid:NCT07220031

Link: https://clinicaltrials.gov/ct2/show/NCT07220031

Conditions:Osmolality Disturbance|Lab Interference
Interventions:Activated Charcoal
Phase:
Title:Activates Charcoal for Patients Undergoing Invasive Procedure Delayed Due to Direct Oral Anticoagulants
Status:Withdrawn
updateDate:2025-10-07
Ctid:NCT02969746

Link: https://clinicaltrials.gov/ct2/show/NCT02969746

Conditions:Anticoagulants; Circulating, Hemorrhagic Disorder
Interventions:Activated Charcoal
Phase:Phase 4
Title:Phase 2 Trial to Evaluate Safety and Immunogenicity of Inventprise's (IVT) 25-valent Pneumococcal Conjugate Vaccine (IVT PCV-25) in Healthy Infants
Status:Active, not recruiting
updateDate:2025-09-02
Ctid:NCT06790290

Link: https://clinicaltrials.gov/ct2/show/NCT06790290

Conditions:Pneumococcal Disease, Invasive
Interventions:Prevnar20
Phase:Phase 2
Title:Activated Charcoal Use in Chronic Kidney Disease Patients
Status:Recruiting
updateDate:2025-08-08
Ctid:NCT06906874

Link: https://clinicaltrials.gov/ct2/show/NCT06906874

Conditions:End Stage Renal Disease (ESRD)|CKD 5D, Hemodialysis|CKD-MBD - Chronic Kidney Disease Mineral and Bone Disorder
Interventions:Phosphate Binders
Phase:Phase 2
Title:Ultrasound Guided Fluid Loading Before Spinal Anesthesia
Status:Completed
updateDate:2025-08-07
Ctid:NCT07108881

Link: https://clinicaltrials.gov/ct2/show/NCT07108881

Conditions:Cesarean Section Complications|Spinal Anesthesia|Hypotension|Hypovolemia|Sympathetic Blockade|Fluid Loading
Interventions:T
Phase:Phase 4
Title:Effect of Injection Duration of Fascial Plane Blocks on Block Success
Status:Not yet recruiting
updateDate:2025-07-31
Ctid:NCT07096765

Link: https://clinicaltrials.gov/ct2/show/NCT07096765

Conditions:Nerve Block
Interventions:Group C
Phase:N/A
Title:Incentive Spirometer Training and Oropharyngeal Motor Training for Pulmonary Dysfunction in Spastic Diplegic Children
Status:Active, not recruiting
updateDate:2025-02-03
Ctid:NCT06806007

Link: https://clinicaltrials.gov/ct2/show/NCT06806007

Conditions:Pulmonary Dysfunction|Spastic Diaplegia
Interventions:Group C
Phase:Early Phase 1
Title:Study to Assess the Taste Profile of Different ALS-008176 Oral Liquid Formulations in Healthy Adult Participants
Status:Completed
updateDate:2025-02-03
Ctid:NCT02813460

Link: https://clinicaltrials.gov/ct2/show/NCT02813460

Conditions:Healthy
Interventions:Formulation H3 (ALS-008176)
Phase:Phase 1
Title:A Value-Driven Study on Reducing Immune Checkpoint Inhibitor Dosing Frequency in Advanced Cancers
Status:Recruiting
updateDate:2025-01-10
Ctid:NCT06422403

Link: https://clinicaltrials.gov/ct2/show/NCT06422403

Conditions:Carcinoma, Hepatocellular|Gastric Adenocarcinoma|GastroEsophageal Cancer|Oesophageal Cancer|Non-small Cell Lung Cancer|Head and Neck Squamous Cell Carcinoma
Interventions:Standard of Care - C
Phase:Phase 2
Title:The Effect of Probiotics vs Activated Charcoal in the Management of CKD Patients Suffering From Uremic Pruritus.
Status:Not yet recruiting
updateDate:2024-08-30
Ctid:NCT06579066

Link: https://clinicaltrials.gov/ct2/show/NCT06579066

Conditions:Chronic Kidney Disease|Uremic Pruritus
Interventions:Activated Charcoal
Phase:Phase 2
Title:Postoperative Analgesia in Laparoscopic Gynecological Surgeries
Status:Not yet recruiting
updateDate:2024-07-09
Ctid:NCT06491485

Link: https://clinicaltrials.gov/ct2/show/NCT06491485

Conditions:Postoperative Pain
Interventions:Group C (lidocaine with saline)
Phase:Phase 4
Title:Does a Soft Drink Mixture Improve Tolerance of Activated Charcoal in the Adult Poisoned Patient Without Affecting Efficacy
Status:Completed
updateDate:2024-05-30
Ctid:NCT06219967

Link: https://clinicaltrials.gov/ct2/show/NCT06219967

Conditions:Overdose
Interventions:Activated Charcoal
Phase:Phase 4
Title:The Efficiency of Preoperative Pericapsular Nerve Group Block Applied With Ultrasound and Success of Spinal Anesthesia
Status:Completed
updateDate:2024-04-26
Ctid:NCT06209372

Link: https://clinicaltrials.gov/ct2/show/NCT06209372

Conditions:Efficiency|Spinal Anesthesia|Block
Interventions:Group C
Phase:
Title:Effect of Dexmedetomidine on Oxygenation and Lung Mechanics
Status:Unknown status
updateDate:2024-04-10
Ctid:NCT06355960

Link: https://clinicaltrials.gov/ct2/show/NCT06355960

Conditions:Drug Use|Dexmedetomidine
Interventions:GROUP C
Phase:N/A
Title:Preoperative Dexamethasone to Improve Quality of Recovery After Laparoscopic Bariatric Surgery
Status:Completed
updateDate:2023-09-21
Ctid:NCT05752734

Link: https://clinicaltrials.gov/ct2/show/NCT05752734

Conditions:Anesthesia|Analgesia|Acute Pain
Interventions:Group C
Phase:
Title:Safety and Efficacy of Artesunate & Curcumin in Crohn's Disease
Status:Unknown status
updateDate:2023-05-23
Ctid:NCT04713631

Link: https://clinicaltrials.gov/ct2/show/NCT04713631

Conditions:Crohn's Disease
Interventions:Placebo C
Phase:Phase 2
Title:AD109 Dose Finding in Mild to Moderate OSA
Status:Completed
updateDate:2022-12-22
Ctid:NCT04631107

Link: https://clinicaltrials.gov/ct2/show/NCT04631107

Conditions:Obstructive Sleep Apnea
Interventions:Placebo- C
Phase:Phase 2
Title:Non Inferiority Study of a Reduced Dose of Activated Charcoal on Rivaroxaban Pharmacokinetics.
Status:Completed
updateDate:2022-12-05
Ctid:NCT04767776

Link: https://clinicaltrials.gov/ct2/show/NCT04767776

Conditions:Healthy
Interventions:Activated charcoal
Phase:Phase 1
Title:Evaluation of Protective Effect of Activated Charcoal and Probiotic Against Progression of Chronic Kidney Disease
Status:Unknown status
updateDate:2022-09-14
Ctid:NCT05540431

Link: https://clinicaltrials.gov/ct2/show/NCT05540431

Conditions:Uremic Toxin
Interventions:Probiotic
Phase:Phase 2/Phase 3
Title:Ultrasound-guided Greater Occipital Nerve Block in Children Undergoing Posterior Fossa Craniotomy
Status:Completed
updateDate:2022-08-15
Ctid:NCT03762343

Link: https://clinicaltrials.gov/ct2/show/NCT03762343

Conditions:Posterior Fossa Tumor
Interventions:control group C
Phase:Phase 3
Title:Study To Determine Bioavailability of Sotagliflozin in Healthy Male and Female Subjects
Status:Completed
updateDate:2022-04-25
Ctid:NCT03802487

Link: https://clinicaltrials.gov/ct2/show/NCT03802487

Conditions:Type 2 Diabetes Mellitus|Healthy Subjects
Interventions:Charcoal
Phase:Phase 1
Title:Charcoal in Lung Cancer Patients Undergoing TEMLA
Status:Withdrawn
updateDate:2022-02-09
Ctid:NCT04928950

Link: https://clinicaltrials.gov/ct2/show/NCT04928950

Conditions:Lung Cancer
Interventions:Activated charcoal
Phase:Phase 2
Title:Post Operative Pain Control for Distal Radius Surgery: Does Exparel Injected at the Surgery Site Improve Postoperative Pain Scores at 24 and 48 Hours ?
Status:Withdrawn
updateDate:2021-10-29
Ctid:NCT04540848

Link: https://clinicaltrials.gov/ct2/show/NCT04540848

Conditions:Post Operative Pain
Interventions:Group C(supraclavicular block only)
Phase:Phase 4
Title:A Study to Evaluate the Safety and Immunogenicity of an Adjuvanted RSV Vaccine in Healthy Older Adults
Status:Terminated
updateDate:2021-08-26
Ctid:NCT03572062

Link: https://clinicaltrials.gov/ct2/show/NCT03572062

Conditions:Respiratory Tract Infection
Interventions:Placebo
Phase:Phase 2
Title:Efficacy of a Synthetic Vaccine Derived From Plasmodium Vivax Circumsporozoite Protein (PvCS) in naïve and Semi-immune Volunteers
Status:Unknown status
updateDate:2021-03-01
Ctid:NCT04739917

Link: https://clinicaltrials.gov/ct2/show/NCT04739917

Conditions:Malaria, Vivax
Interventions:Vaccine PvCS N+C+R 150 mcg
Phase:Phase 2
Title:A Randomized, Open-label, Single-dose, Single-center, Crossover Study in Healthy Subjects to Assess the Relative Bioavailability of PT010
Status:Completed
updateDate:2020-06-11
Ctid:NCT03311373

Link: https://clinicaltrials.gov/ct2/show/NCT03311373

Conditions:Chronic Obstructive Pulmonary Disease
Interventions:Regimen D
Phase:Phase 1
Title:Role of Activated Charcoal in Decreasing Blood Urea, Creatinine and Phosphorous
Status:Unknown status
updateDate:2020-05-14
Ctid:NCT04311645

Link: https://clinicaltrials.gov/ct2/show/NCT04311645

Conditions:Chronic Kidney Disease stage3
Interventions:Dry seeds
Phase:Phase 2
Title:An Efficacy and Safety Study of Ha44 Gel Administered Topically for the Treatment of Head Lice Infestation
Status:Completed
updateDate:2020-04-29
Ctid:NCT01336647

Link: https://clinicaltrials.gov/ct2/show/NCT01336647

Conditions:Pediculosis
Interventions:Group C - Placebo
Phase:Phase 2
Title:Effect of Nutrition Ingredients on Microbiota Modulation
Status:Completed
updateDate:2020-03-30
Ctid:NCT03668964

Link: https://clinicaltrials.gov/ct2/show/NCT03668964

Conditions:Healthy Volunteers
Interventions:Placebo
Phase:N/A
Title:Find the Adequate Dose of Nalbuphine for Laparoscopic Cholecystectomy
Status:Unknown status
updateDate:2019-10-22
Ctid:NCT04135534

Link: https://clinicaltrials.gov/ct2/show/NCT04135534

Conditions:Post Operative Pain|Opioid Side Effects
Interventions:group C
Phase:N/A
Title:Study to Evaluate Safety/Duration in Stomach of Extended Release Capsules in Healthy Adults
Status:Completed
updateDate:2019-02-26
Ctid:NCT03718390

Link: https://clinicaltrials.gov/ct2/show/NCT03718390

Conditions:Gastric Retention|Healthy
Interventions:Formulation E
Phase:Early Phase 1
Title:A Study to Evaluate the Effect of Activated Charcoal on the Absorption of LY2216684 in Healthy Subjects
Status:Completed
updateDate:2019-01-04
Ctid:NCT01389752

Link: https://clinicaltrials.gov/ct2/show/NCT01389752

Conditions:Depressive Disorder, Major
Interventions:Activated Charcoal
Phase:Phase 1
Title:Allogeneic Hematopoietic Stem Cell Transplantation With Reduced Intensity Pre-transplant Conditioning for the Treatment of High-risk Hematological Malignancies (V3)
Status:Terminated
updateDate:2018-07-11
Ctid:NCT01139164

Link: https://clinicaltrials.gov/ct2/show/NCT01139164

Conditions:Hematological Malignancies
Interventions:Regimen C
Phase:Phase 2
Title:Study to Evaluate Taste Profile of Different JNJ-53718678 Oral Liquid Formulations in Healthy Participants
Status:Completed
updateDate:2018-05-15
Ctid:NCT02426632

Link: https://clinicaltrials.gov/ct2/show/NCT02426632

Conditions:Healthy
Interventions:Formulation N3
Phase:Phase 1
Title:Evaluation of the Protective Efficacy of a Vaccine Derived From the Synthetic CS Protein of Plasmodium Vivax
Status:Completed
updateDate:2018-03-23
Ctid:NCT02083068

Link: https://clinicaltrials.gov/ct2/show/NCT02083068

Conditions:Malaria
Interventions:SSN Montanide ISA-51
Phase:Phase 2
Title:An Open Label Study to Examine the Effects of a High-Fat Meal and Particle Size on the Pharmacokinetics of Orally Administered GSK2118436 in Subjects With BRAF Mutation Positive Tumor
Status:Completed
updateDate:2017-11-14
Ctid:NCT01231568

Link: https://clinicaltrials.gov/ct2/show/NCT01231568

Conditions:Cancer
Interventions:Regimen D
Phase:Phase 1
Title:Bioequivalence and Food Effect Study in Healthy Volunteers
Status:Completed
updateDate:2017-08-07
Ctid:NCT00495274

Link: https://clinicaltrials.gov/ct2/show/NCT00495274

Conditions:Sleep Initiation and Maintenance Disorders
Interventions:Formulation G
Phase:Phase 1
Title:Firategrast (SB683699) Surface Area Study in Multiple Sclerosis Patients
Status:Completed
updateDate:2017-08-01
Ctid:NCT00548769

Link: https://clinicaltrials.gov/ct2/show/NCT00548769

Conditions:Multiple Sclerosis
Interventions:Formulation D
Phase:Phase 1
Title:Prophylaxy of Postoperative Nausea and Vomiting in Patients Undergoing Laparoscopic Surgery
Status:Unknown status
updateDate:2017-06-28
Ctid:NCT03202459

Link: https://clinicaltrials.gov/ct2/show/NCT03202459

Conditions:Postoperative Complications|Postoperative Nausea and Vomiting
Interventions:Group C - placebo
Phase:N/A
Title:Healthy Volunteer Pilot Study Using 3 Types of Modified Release Formulations of Firategrast to Investigate How Quickly Absorption From the Digestive System Takes Place.
Status:Completed
updateDate:2017-06-20
Ctid:NCT01424462

Link: https://clinicaltrials.gov/ct2/show/NCT01424462

Conditions:Multiple Sclerosis, Relapsing-Remitting
Interventions:D
Phase:Phase 1
Title:Multiple Ascending Oral Dose Study of F901318 in Healthy Subjects
Status:Completed
updateDate:2017-05-23
Ctid:NCT02737371

Link: https://clinicaltrials.gov/ct2/show/NCT02737371

Conditions:Invasive Aspergillosis
Interventions:Placebo Dose level C oral
Phase:Phase 1
Title:Study to Evaluate the Safety, Tolerability and Pharmacokinetics of GSK2269557 Administered Via the ELLIPTA Dry Powder Inhaler to Healthy Subjects
Status:Completed
updateDate:2017-04-26
Ctid:NCT02691325

Link: https://clinicaltrials.gov/ct2/show/NCT02691325

Conditions:Pulmonary Disease, Chronic Obstructive
Interventions:Activated charcoal
Phase:Phase 1
Title:Conventional Fasting Versus Lipid/Carbohydrate Infusion for Coronary Bypass Patients
Status:Completed
updateDate:2017-01-27
Ctid:NCT03033667

Link: https://clinicaltrials.gov/ct2/show/NCT03033667

Conditions:Metabolism Disorder
Interventions:Group C
Phase:N/A
Title:A Study to Compare the Effects of Different Sized Particles on Cells in the Nose
Status:Completed
updateDate:2017-01-11
Ctid:NCT01257191

Link: https://clinicaltrials.gov/ct2/show/NCT01257191

Conditions:Hypersensitivity, Immediate|Atopic Hypersensitivity
Interventions:Saline
Phase:Phase 1
Title:A Study on The Effect of Multiple Doses of Activated Charcoal on The Pharmacokinetics of a Single Dose of RO4995819
Status:Completed
updateDate:2016-11-02
Ctid:NCT01409369

Link: https://clinicaltrials.gov/ct2/show/NCT01409369

Conditions:Healthy Volunteer
Interventions:activated charcoal
Phase:Phase 1
Title:Optimizing Dosing Regimen of Piperacillin/Tazobactam for Nosocomial Pneumonia
Status:Unknown status
updateDate:2016-02-17
Ctid:NCT01796717

Link: https://clinicaltrials.gov/ct2/show/NCT01796717

Conditions:Nosocomial Pneumonia
Interventions:E Group
Phase:Phase 2/Phase 3
Title:Immunogenicity and Safety of Group A, C, Y and W135 Meningococcal Polysaccharide Vaccine
Status:Completed
updateDate:2015-09-22
Ctid:NCT02003313

Link: https://clinicaltrials.gov/ct2/show/NCT02003313

Conditions:Meningitis
Interventions:Group C
Phase:Phase 3
Title:Ribavirin Loading Dose or Priming and Concentration Targeting for HCV Genotype 1
Status:Completed
updateDate:2015-03-24
Ctid:NCT01226771

Link: https://clinicaltrials.gov/ct2/show/NCT01226771

Conditions:Hepatitis C
Interventions:Group C ('Standard-of-Care')
Phase:Phase 3
Title:Effect of Teriflunomide on Immune Cell Subsets in the Blood of Patients With Multiple Sclerosis
Status:Completed
updateDate:2015-03-13
Ctid:NCT01863888

Link: https://clinicaltrials.gov/ct2/show/NCT01863888

Conditions:Multiple Sclerosis
Interventions:charcoal
Phase:Phase 3
Title:Dose-Escalate Study to Investigate the Safety and Tolerability of T89 in Japanese
Status:Completed
updateDate:2014-11-24
Ctid:NCT01679028

Link: https://clinicaltrials.gov/ct2/show/NCT01679028

Conditions:Healthy
Interventions:T89 Group C
Phase:Phase 1
Title:Phenytoin and Multidose Activated Charcoal
Status:Completed
updateDate:2014-09-11
Ctid:NCT00823264

Link: https://clinicaltrials.gov/ct2/show/NCT00823264

Conditions:Phenytoin Toxicity
Interventions:Activated Charcoal
Phase:N/A
Title:Migalastat Food Effect Study
Status:Completed
updateDate:2013-12-18
Ctid:NCT01489995

Link: https://clinicaltrials.gov/ct2/show/NCT01489995

Conditions:Fabry Disease
Interventions:E (migalastat)
Phase:Phase 1
Title:A Drug Interaction Study of Cilnidipine and Valsartan
Status:Completed
updateDate:2013-10-14
Ctid:NCT01838967

Link: https://clinicaltrials.gov/ct2/show/NCT01838967

Conditions:Healthy
Interventions:C+V - V - C
Phase:Phase 1
Title:Phase 3 Study of A Group A, C Polysaccharide Meningococcal and Type b Haemophilus Influenzal Conjugate Vaccine
Status:Completed
updateDate:2013-05-08
Ctid:NCT01580033

Link: https://clinicaltrials.gov/ct2/show/NCT01580033

Conditions:Meningitis|Influenza
Interventions:Hib vaccine
Phase:Phase 3
Title:Tranexamic Acid Versus Placebo for the Reduction of Blood Loss in Total Hip Replacement Surgery
Status:Completed
updateDate:2013-02-07
Ctid:NCT01199627

Link: https://clinicaltrials.gov/ct2/show/NCT01199627

Conditions:Hip Replacement, Total
Interventions:C
Phase:Phase 3
Title:Effect of Lidocaine Sprayed on Hemodynamics During Endotracheal Intubation
Status:Unknown status
updateDate:2012-11-29
Ctid:NCT01737437

Link: https://clinicaltrials.gov/ct2/show/NCT01737437

Conditions:Neurosurgical Patients
Interventions:group LV
Phase:N/A
Title:Adjunctive Supplementation of Antioxidants (Vitamins E + C) Plus Omega-3 Fatty Acids
Status:Terminated
updateDate:2012-10-24
Ctid:NCT00211562

Link: https://clinicaltrials.gov/ct2/show/NCT00211562

Conditions:Schizophrenia
Interventions:Olanzapine, Omega 3, Vitamin E+C
Phase:Phase 3
Title:Immunogenicity and Safety of A Group A, C Polysaccharide Meningococcal and Type b Haemophilus Influenzal Conjugate Vaccine in Infants and Children
Status:Completed
updateDate:2012-04-19
Ctid:NCT01428908

Link: https://clinicaltrials.gov/ct2/show/NCT01428908

Conditions:Group A, C Polysaccharide Meningitis|Type b Haemophilus Influenza
Interventions:Hib vaccine
Phase:Phase 3
Title:Treatment of Schizophrenia With an Omega-3 Fatty Acid (EPA) and Antioxidants
Status:Completed
updateDate:2011-01-04
Ctid:NCT00419146

Link: https://clinicaltrials.gov/ct2/show/NCT00419146

Conditions:Schizophrenia|Schizophreniform Disorders|Schizoaffective Disorder|Psychotic Disorders
Interventions:Vitamins E + C
Phase:Phase 2/Phase 3
Title:Calcium, Dairy, and Body Fat in Adolescents
Status:Completed
updateDate:2010-01-13
Ctid:NCT00592137

Link: https://clinicaltrials.gov/ct2/show/NCT00592137

Conditions:Obesity|Energy Metabolism
Interventions:A (smoothies based on dairy protein containing calcium)
Phase:N/A

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