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临床试验/CTRI/2025/09/094655
CTRI/2025/09/094655尚未招募2 期

Comparative Clinical Evaluation of Jeevantyadi Ghrit and Mahatriphaladi Ghrit Tarpan with Saptamrit Lauh Orally in Pratham Patalgata Timir

Patanjali Bhartiya Ayurvigyan Evam Anusandhan Sansthan ,Haridwar1 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23日最近更新:

试验速览

阶段
2 期
状态
尚未招募
发起方
入组人数
60
试验地点
1
主要终点
Assessment will be done on the basis of Subjective parameter

研究概览

简要总结

In this trial, patients diagnosed with Pratham Patalgata Timir will be selected and randomly divided into two groups, with 30 patients in each group.

Group A Patients will receive the Ayurvedic procedure of Tarpan with Jeevantyadi Ghrit, along with oral administration of Saptamrit Lauh.

Group B Patients will receive the Ayurvedic procedure of Tarpan with Mahatriphaladi Ghrit, along with oral administration of Saptamrit Lauh.

Assessment will be carried out on the basis of both subjective and objective parameters. One follow-up will be conducted 30 days after the completion of treatment.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
None

入排标准

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

入选标准

  • Patient with symptoms of Simple myopia.
  • Patient between the age group 8 to 40 years of either sex.
  • Patients who are fit for Tarpan karma.
  • Patient having lakshanas of Pratham Patalgata Timir.
  • Patients with refractive error less than 6D.

排除标准

  • 1.Patient less than 8 year of age and above 40 year of age.
  • 2.Patient suffering from any other systemic disease and receiving medicine for the same.
  • 3.Patients who are unfit for Tarpan karma.
  • 4.Patients with refractive error more than 6D.

结局指标

主要结局

Assessment will be done on the basis of Subjective parameter

时间窗: Baseline (before treatment); End of treatment (4 weeks, primary time point)

1 Avyaktani sa rupani

时间窗: Baseline (before treatment); End of treatment (4 weeks, primary time point)

2 Strain in eyes

时间窗: Baseline (before treatment); End of treatment (4 weeks, primary time point)

3 Headache

时间窗: Baseline (before treatment); End of treatment (4 weeks, primary time point)

次要结局

  • Assessment will be done on the basis of Objective parameters(Objective parameters)

研究者

发起方
Patanjali Bhartiya Ayurvigyan Evam Anusandhan Sansthan ,Haridwar
申办方类型
Private medical college
责任方
Principal Investigator
主要研究者

Shan Chandel

Patanjali Bhartiya Ayurvigyan Evam Anusandhan Sansthan ,Haridwar

研究点 (1)

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