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临床试验/CTRI/2025/09/094799
CTRI/2025/09/094799尚未招募3 期

COMPARATIVE CLINICAL EVALUATION OF MANIBHADRA LEHA WITH AND WITHOUT PANCHATIKTA GHRITA MATRA BASTI IN EKKUSTHA PSORIASIS

Patanjali Bhartiya Ayurvigyan Evam Anusandhan1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年9月27日最近更新:

试验速览

阶段
3 期
状态
尚未招募
发起方
入组人数
60
试验地点
1
主要终点
change in clinical presentation of psoriasis assess through

研究概览

简要总结

This is an open label, comparative clinical trial to evaluate the efficacy of Manibhadra Leha with and without Panchtikta Ghrita Matra Basti in Psoriasis. A total number of 60 patient fulfilling the inclusion criteria  will be randomly divided into 30 each. One group will be recieving Manibhadra Leha for 30 days and other will be recieving Manibhadra Leha for 23 days with Panchtikta Ghrita Matra Basti  for 7 days.The efficacy will be assessed based on subjective symptoms like itching, erythema, scaling and PASI score along with CDQLI scale. Follow up will be done on 7th,15th,30th and 45th day of study. The aim is to compare both regimens and provide a cost effective, safe, and efficient ayurvedic intervention for Psoriasis.

研究设计

研究类型
Interventional
分配方式
Coin toss, Lottery, toss of dice, shuffling cards etc
盲法
None

入排标准

年龄范围
5.00 Year(s) 至 16.00 Year(s)(—)
性别
All

入选标准

  • Children aged between 5-16 years Patients of either sex Children having classical sign and symptoms of psoriasis.

排除标准

  • Patients below 5 years of age and above 16 years of age Patient suffering from any other chronic systemic illness and allergic disorders Patient diagnosed with any other skin disorder except psoriasis Patient not fulfilling the inclusion criteria Patient and attendant not willing to given written consent for participation Patient with any complication of psoriasis example pustular psoriasis psoriasis with arthritis.

结局指标

主要结局

change in clinical presentation of psoriasis assess through

时间窗: Base line assessment day0 | mid treatment assessment day15 | post treatment assessment day45

1. PASI Score

时间窗: Base line assessment day0 | mid treatment assessment day15 | post treatment assessment day45

2. CDQLI Score

时间窗: Base line assessment day0 | mid treatment assessment day15 | post treatment assessment day45

3. Improvement in subjective parameter like itching,scaling,erythema

时间窗: Base line assessment day0 | mid treatment assessment day15 | post treatment assessment day45

4. Change in subjective parameter like Auspitz sign, candle grease sign

时间窗: Base line assessment day0 | mid treatment assessment day15 | post treatment assessment day45

次要结局

  • Improvement in scar and itching and Improvement in over all health of the patient(45 days)

研究者

发起方
Patanjali Bhartiya Ayurvigyan Evam Anusandhan
申办方类型
Research institution and hospital
责任方
Principal Investigator
主要研究者

Sakshi choudhary

Patanjali Bhartiya Ayurvigyan Evam Anusandhan Sansthan

研究点 (1)

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