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临床试验/CTRI/2013/12/004262
CTRI/2013/12/004262招募中2 期

Clinical Validation of Unani Pharmacopoeal formulation Tiryaq-e-Pachish in Zaheer (Dysentery)

Monetary Support Central Council for Research in Unani Medicine CCRUM New Delhi2 个研究点 分布在 1 个国家目标入组 170 人开始时间: 2011年2月11日最近更新:
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试验速览

阶段
2 期
状态
招募中
发起方
入组人数
170
试验地点
2
主要终点
Improvement in signs and symptoms
研究概览研究设计入排标准结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

This study is designed as a multicentric open trial in patients with Zaheer(Dysentry). After screening, Patients will be enrolled if they satisfy inclusion and exclusion criteria.  The clinical follow-up will be carried out every alternate day.This includes subjective assessment of general well being and physical examination. The total duration of treatment will be 01 week. Laboratory parameters for safety assessment will be conducted at baseline and end of study.

研究设计

研究类型
Interventional
分配方式
Not Applicable
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

  • •â€¢Age-20-60 •Increased frequency of motion •Tenesmus •Sense of incomplete evacuation •Frequent constipation followed by diarrhoea •Loose stools with or without mucous •Associated symptoms like Nausea /Flatulence /Vomiting.

排除标准

  • •1Patients with severe loose motion more than 8 in a day 2Patients with blood in stool 3Cholera/Ulcerative colitis 4High grade fever (more than 101 ºC) 5Patient having illnesses requiring long term treatment especially DM, CRF,HT.

结局指标

主要结局

Improvement in signs and symptoms

时间窗: 1 WEEK

次要结局

  • Hematological and biochemical assessments for safety(1 WEEK)

研究者

发起方
Monetary Support Central Council for Research in Unani Medicine CCRUM New Delhi
申办方类型
Research institution

研究点 (2)

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