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临床试验/CTRI/2025/06/089796
CTRI/2025/06/089796尚未招募2/3 期

Randomized comparative clinical study of Shunthyadi Churna Vati with Triphala Guggul Vati in post-operative pain management after open fistulectomy in Bhagandara (Fistula in Ano) in the age group 18-60 years.

Dayabhai Maoji Majithiya Ayurved Mahavidyalaya, Yavatmal1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2025年5月7日最近更新:

试验速览

阶段
2/3 期
状态
尚未招募
发起方
入组人数
70
试验地点
1
主要终点
Patients suffering from post-operative pain after open fistulectomy in Bhagandara (Fistula in Ano).

研究概览

简要总结

The current study is randomized controlled clinical to study the efficacy of Shunthyadi Churna Vati in post operative pain management after open fistulectomy in bhagandara ( Fistula in ano).  Post operated patients of open fistulectomy will be divided into two equal groups experimental and controlled. The treatment for experimental group is Shunthyadi Churna Vati for 21 days and for controlled group is Triphala Guggul Vati for 21 days. Assessment will be done on 0, 3rd, 5th, 7th, 14th, 21st and 28th day.

研究设计

研究类型
Interventional
分配方式
Coin toss, Lottery, toss of dice, shuffling cards etc
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

  • Post-operated patients of open fistulectomy of Fistula in Ano.
  • Age group above 18 and below 60 years.
  • Patients willing for a clinical trial, Irrespective of gender, occupation, religion, and economic barriers.
  • Patients with controlled DM and Hypertension.
  • 5 Patients who are willing to give written consent.

排除标准

  • 1 Patients having uncontrolled DM and Hypertension, TB, Ulcerative colitis, Crohn’s disease, or any malignancy& Immunocompromised like HIV, HBsAg. 2 Patient on anticoagulant therapy 3 Patients having addictions specifically alcohol, tobacco &smoking.

结局指标

主要结局

Patients suffering from post-operative pain after open fistulectomy in Bhagandara (Fistula in Ano).

时间窗: 0,3rd,5th,7th,14th,21st,28th

次要结局

  • 1.Visual analogue scale(2.tenderness)

研究者

发起方
Dayabhai Maoji Majithiya Ayurved Mahavidyalaya, Yavatmal
申办方类型
Research institution and hospital

研究点 (1)

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