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临床试验/CTRI/2026/02/105031
CTRI/2026/02/105031尚未招募不适用

Effect of selected Ayurveda treatment protocol in Varicose veins : A single arm clinical trial

Haritha P V1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2026年3月18日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
40
试验地点
1

研究概览

简要总结

The study is designed as a pre and post interventional study without a control group involving a sample size of 40 participants. Participants between the age group of 40 to 60 years irrespective of gender having Varicose veins satisfying inclusion and exclusion criteria will be consecutively selected from the OPD and IPD Dept. of Shalyatantra Govt. Ayurveda College Thiruvananthapuram. The treatment protocol includes internal administration of Sahacharadi Kashaya Kaisora Guggulu Tablet Sahacharadi Sevya Thailam and external application of Sahacharadi Thailam for a period of 35 days along with Siravedha done on 28th day. Assessment will be done by Venous Clinical Severity Score on 0th,14th, 28th and 35th day, and Venous Blood Gas analysis on 0th and 35th day. The findings will be recorded and the result will be statistically analysed according to the nature of data using Paired t test or Wilcoxon Signed Rank test.

研究设计

研究类型
Interventional

入排标准

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

入选标准

  • C4-C5 of CEAP Classification of Varicose veins.

排除标准

  • Participants with bleeding disorders Participants with Anaemia Participants testing positive for HIV HCV HBsAg VDRL Participants with uncontrolled DM and HTN Pregnant and lactating mothers Those who are contraindicated for siravedha.

研究者

发起方
Haritha P V
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr Subi N H

Government Ayurveda College Thiruvananthapuram

研究点 (1)

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