CTRI/2021/05/033903已完成1 期
An Open-Label, Balanced, Randomized, Single-Dose, Four Treatment, Four Period, Four Sequence, Four Way Crossover Study of Oral Bioavailability of Sundalp/Micellon Standardized To Min. 2.25% Curcuminoids Capsules 500 mg1 Soft gel Capsule of Manufactured By Sferalp SAVia Cantonale 77, CH-6998 Monteggio, Switzerland T1, Sundalp/ Micellon Standardized To Min. 2.25% Curcuminoids Capsules 2000 Mg 4*500 mg Soft gel Capsules of Manufactured By Sferalp SA Via Cantonale 77, CH-6998 Monteggio, Switzerland T2 with Curcumin Phytosome 500 Mg Turmeric Rhizome Extract Curcuma Longa Phosphatidyl Choline Complex Meriva Turmeric PhytosomeStandardized To Min. 18% Curcuminoids 90 Mg 1 Capsule Manufactured By Now Foods 395 S. Glen Ellyn Rd., Bloomingdale, IL 60108, USA R1, Jigsaw Health Curcumin C 3 Complex 500 Mg NLT 95% Total Curcuminoids Curcuma Longa Rhizomes 1 Capsule Manufactured By Jigsaw Health LLC 9035 E Pima Center Pkwy Suite 4 Scottsdale AZ 85258 USA R2 - In Healthy, Adult, Human Subjects Under Fasting Conditions
Pharmabase SA0 个研究点目标入组 24 人开始时间: 待定最近更新:
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 发起方
- 入组人数
- 24
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Ba/be
入排标准
入选标准
- •Normal healthy human adult subjects of age 18-45 years with BMI between 18.5 kg/m2 to 29.99 kg/m2
- •Subjects whose screening laboratory values are within normal limits or considered by the physician or principal/clinical investigator to be of no clinical significance
- •Healthy as documented by the medical history, physical examination (including but may not be limited to an evaluation of the cardiovascular, gastrointestinal, respiratory, musculoskeletal and central nervous systems) and vital sign assessments.
- •Generally healthy as documented by 12-lead electrocardiogram (ECG), X-Ray and clinical laboratory assessments.
- •Willing to consume ova lacto vegeterian diet
排除标准
- •Evidence of allergy or known hypersenstivity to curcumin or its inactive ingredients.
- •Renal or liver impairment.
- •Any disease or condition which might compromise the haemopoeitic, gastrointestinal, renal, hepatic, cardiovascular, Musculoskeletal, respiratory, central nervous system, diabetes, psychosis or any other body system.
- •History of alcohol addiction or abuse.
- •Consumption of caffeine and /or Xanthine containing products (i.e. coffee, tea, chocolate, and caffeine-containing sodas, colas, etc.) tobacco containing products for at least 48.00 hours prior to check-inand throughout the entire study.
- •Consumption of alcohol and its products, grapefruit and/ or its juice and poppy containing foods within 72.00 hours prior to check-inand throughout the entire study.
- •History difficulty in swallowing, accessibility of veins.
研究者
相似试验
尚未招募
不适用
Bioequivalence Study of Sulfadoxine/Pyrimethamine 500 mg/25 mg Dispersible Tablets in Healthy subjects.CTRI/2018/11/016376Rena Exports
已完成
不适用
Bioequivalence study of Cladribine 10 mg tablet in highly active relapsing multiple sclerosis patientsCTRI/2021/09/036201Hikma Pharmaceuticals40
尚未招募
4 期
To Evaluate Oral Bioavailability Efficacy of Co Enzyme Q10 100mg in Healthy Human Adult SubjectsCTRI/2022/10/046730Doctors Best Inc
尚未招募
不适用
Bioavailability study of Amaryl (glimepiride) Tablet 1 mg in healthy, adult, human subjects under fed conditioCTRI/2022/11/046993Sanofi Healthcare India Private Limited
尚未招募
1 期
Comparative Bioavailability Study of Ketorolac TromethamineSublingual Tablet 10 mg in healthy human subjectsCTRI/2024/05/067180Troikaa Pharmaceuticals Ltd
