CTRI/2009/091/000514已完成3 期
A prospective, open labeled, randomised, comparative efficacy & safety trial of polyherbal formulation WH- 1 with Fluconazole, Tinidazole & FAS-3 kit in female patients with vaginitis.
Dr. V.R. Bapat,Ayurvedic Consultant# 375 First B main.First Phase, Girinagar,Bangalore 560085Tel: 080 ? 26720139E mail : vrbapat@yahoo.co.in0 个研究点目标入组 90 人开始时间: 待定最近更新:
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- 入组人数
- 90
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •After getting the IERB approval.
- •Married women in the age of 18 to 60 years.
- •Patients/Subjects diagnosed to have vaginitis.
- •Subjects proven to be eligible through clinical, biochemical examination.
- •?No clinical evidence of hepatic or renal impairment.
- •?Subjects who have given written informed consent.
- •?Female patients / subjects who have given consent for their partner to be included in trial
排除标准
- •Pregnant & lactating women.
- •Chronic disorder such as cardiac (hypertension uncontrolled, arrhythmia), diabetes and endocrine dysfunction (thyroid uncontrolled) as assessed through clinical examination / lab investigations.
- •Women with multiple partners.?
- •Subjects with h/o smoking, alcohol & drug dependence etc.
- •History of Allergy to herbal medication.
- •Participating in any other study within six weeks preceding day one of the study.
- •?Patients currently on medication such as Metronidazole & other antifungal drugs.
研究者
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