A randomized comparative clinical study to evaluate the efficacy of simhasyadi kwatha and patoladipanchanga kwatha in management of amlapitta - NI

Dr Vijayalakshmi Teggi0 个研究点目标入组 0 人开始时间: 待定最近更新: 2024年7月22日

试验速览

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•1. Subject of either sex.
•2. Subject within the age group 18-60 yrs.
•3. Subjects with clinical features of Amlapitta such as Avipaka, Klama, Uthklesha, Tikta Amlodgara, Gourava, Hruthkanta daha, and Aruchi will be included.
•4. Subjects with controlled systemic disorder such as DM, HTN, etc will be included.
•5. Subjects who are willing to give written consents for the study.

•1. Pregnant and Lactating women
•2. Subjects with uncontrolled systemic disorder such as Diabetes mellitus, Hypertension, etc
•3. Subject diagnosed with Gastro- intestinal disorders like peptic ulcer, pancreatic and hepatic disorders.
•4. Subjects with history of haematemesis, malena and other systemic disorders that may interfere with the clinical trial.

发起方

Dr Vijayalakshmi Teggi