临床试验/CTRI/2024/12/078679

CTRI/2024/12/078679尚未招募2 期

A RANDOMISED CLINICAL TRIAL ON COMPARATIVE EFFICACY OF PUTIKADI LEPA AND SHVITRAHARA VARTI COADMINISTERED WITH SHASHILEKHA VATI IN VITILIGO PATIENTS AND ITS IMPACT ON ALPHA-MSH.

ALL INDIA INSTITUTE OF AYURVEDA1 个研究点分布在 1 个国家目标入组 72 人开始时间: 2025年1月1日最近更新: 2024年10月28日

试验速览

阶段: 2 期
状态: 尚未招募
发起方: ALL INDIA INSTITUTE OF AYURVEDA
入组人数: 72
试验地点: 1
主要终点: improvement in shwitra assessed through VETF and VASI score in vitiligo patients.

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

The clinical efficacy of Sashilekha Vatiand Shvitrahar Vartiare documented in previous studies. However, no combination study of the two drugs is yet available.The ointment Putikadi Lepa[i] is a classical yoga mentioned in Sushruta Samhita 940 for Shvitra.No previous study on Putikadi Lepa in relation to Shvitra is yet available across various research databases, hence this drug was chosen to compare its effectiveness with Shvitrahar Varti througha clinical trial of 60 days.

研究设计

研究类型: Interventional
分配方式: Randomized

入排标准

年龄范围: 21.00 Year(s) 至 45.00 Year(s)（—）
性别: All

入选标准

•(1) Patients diagnosed with nonsegmental vitiligo with maximum 2 years of disease history.
•(2) Patients of age group: 21-45 years of either gender.
•(3) Patients willing to participate.

排除标准

•(1) Patients suffering from psychiatric illness.
•(2) Pregnant females and lactating women.
•(3) Patients suffering from any other Systemic Disorders like uncontrolled diabetes, hepatitis B positive, HIV positive, active case of tuberculosis, immunocompromised patient, kidney disease, other skin disease.
•(4) Cases of vitiligo due to burns.
•(5) Any allergic condition related to skin and hypersensitivity to any medicine.

结局指标

主要结局

improvement in shwitra assessed through VETF and VASI score in vitiligo patients.

时间窗: 0th day and 60th day.

次要结局

change in level of Alpha-MSH at 0th to 60th day in blood samples of vitiligo patients(0th day to 60th day)

研究者

发起方

ALL INDIA INSTITUTE OF AYURVEDA

申办方类型

Research institution and hospital

责任方

Principal Investigator

主要研究者

VINAY KUMAR

ALL INDIA INSTITUTE OF AYURVEDA, NEW DELHI

研究点 (1)

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