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临床试验/CTRI/2018/01/011628
CTRI/2018/01/011628已完成3 期

Efficacy of Whole System Research Ayurveda Interventions on Irritable Bowel Syndrome –Randomized Controlled Clinical Trail.

Dr Teja D Naik1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2018年10月2日最近更新:

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
40
试验地点
1
主要终点
1.IBS Adequate Relief (IBS-AR)

研究概览

简要总结

Considering lacuna in IBS management and Ayurvedaresearch issues, current study is planned to explore the efficacy of WholeSystem Research(WSR) approach of Ayurveda interventions in IBS.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Not Applicable

入排标准

年龄范围
20.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • 1.Individuals between the age group of 20 to 60 years fulfilling diagnostic criteria for IBS(Rome IV) of either sex.
  • 2.Either sex.

排除标准

  • 1.Patient on any Intervention for IBS in the period of last 4 weeks 2.Patients with known/history of Carcinoma Colon, ulcerative colitis 3.Patients with alcohol dependency or drug dependency.
  • 4.Pregnant or lactating women 5.Patients suffering from major systemic illness necessitating long term drug treatment, Rheumatoid arthritis, tuberculosis, etc.

结局指标

主要结局

1.IBS Adequate Relief (IBS-AR)

时间窗: 60th day

2.IBS Symptom Severity Score (IBS-SSS)

时间窗: 60th day

次要结局

  • 1.Abdominal Pain- VAS (0-10)(2.Stool Consistency- Bristol Stool Form (BSF))

研究者

发起方
Dr Teja D Naik
申办方类型
Research institution and hospital

研究点 (1)

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