CTRI/2018/01/011617已完成Unknown
A Randomized, Double Blind, Placebo Controlled, Four Arm, Parallel Group Study To Evaluate The Comparative Efficacy Of Different Forms And Doses Of Curcumin With That Of A Placebo In Active Rheumatoid Arthritis Patients.
Plant Lipids P Limited1 个研究点 分布在 1 个国家目标入组 48 人开始时间: 2016年2月15日最近更新:
试验速览
- 阶段
- Unknown
- 状态
- 已完成
- 发起方
- 入组人数
- 48
- 试验地点
- 1
- 主要终点
- To evaluate the comparative efficacy of curcumin (low & high dose), white curcumin with that of a placebo
研究概览
简要总结
A randomized, double blind, placebo controlled,four arm, parallel group study To evaluate the comparative efficacy of curcumin(low & high dose), white curcumin with that of a placebo
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18.00 Year(s) 至 60.00 Year(s)（—）
- 性别
- All
入选标准
- •i.Patients with active RA for at least one (1) year, diagnosed according to the revised 1987 American College of Rheumatology (ACR) criteria for the classification of rheumatoid arthritis.
- •ii.Receiving treatment on an outpatient basis.
- •iii.Active disease at the time of screening.
排除标准
- 未提供
结局指标
主要结局
To evaluate the comparative efficacy of curcumin (low & high dose), white curcumin with that of a placebo
时间窗: Screening – (Day - 7) | Baseline visit – (Day 0) | Visit 2 (Day 30) | Visit 3 (Day 60) | Visit 4 (Day 90)
次要结局
- a.To assess the safety & tolerability of active products(b.To assess changes in various biomarkers during the study period among all the study group subjects.)
研究者
研究点 (1)
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