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临床试验/CTRI/2018/04/013122
CTRI/2018/04/013122尚未招募2 期

A prospective open labelled non-randomized phaseII clinical trial to evaluate the therapeutic efficacy of the Siddha medicine "Thiripalai Mathirai" (Internal) for the treatment of Pitha Paandu (Iron Deficiency Anaemia)

Dr S Neelavathi MD Siddha PhD1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2018年4月16日最近更新:

试验速览

阶段
2 期
状态
尚未招募
发起方
入组人数
40
试验地点
1
主要终点
Clinical and Therapeutic efficacy of the siddha medicine Thiripalai Mathirai in Pitha Paandu

研究概览

简要总结

The study is A Prospective Open Labelled Non Randomized Phase 2 Clinical trial to evaluate the therapeutic efficacy of THIRIPALAI MATHIRAI 1 with the adjuvant KARISALAI KUDINEER 100ml BD for 30 days in 40 patients during the trial period of 20 months that will be conducted in Govt Siddha Medical College and Hospital Palayamkottai Tirunelveli Tamilnadu India

The primary outcome will be the therapeutic efficacy of  trial medicine Thiripalai Mathirai with the adjuvant Karisalai kudineer

The secondary outcome will be the evaluation of siddha diagnostic parameters Safety of trial drug and the adjuvant Pharmacological and Biochemical analysis of trial drug and the adjuvant

研究设计

研究类型
Interventional
分配方式
Not Applicable
盲法
Open Label

入排标准

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

入选标准

  • Patients with Hb level between 7 to 10 grams Pallor of skin mucous membrane conjunctiva nailbeds Fatigue Shortness of breath Palpitation Anorexia Worm infestations Blood loss due to Menstrual disorders Hemorrhoids Peptic ulcer Smear showing hypochromic microcytic RBCs.

排除标准

  • Patients with Congenital heart disease Chronic renal disease Liver disease Inherited haemolytic defects Thalessemia Thyroid disorder Diabetes mellitus.

结局指标

主要结局

Clinical and Therapeutic efficacy of the siddha medicine Thiripalai Mathirai in Pitha Paandu

时间窗: 30 days

次要结局

  • Evaluation of siddha diagnostic parameters(Safety of trial drug and the adjuvant)

研究者

发起方
Dr S Neelavathi MD Siddha PhD
申办方类型
Government medical college

研究点 (1)

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