跳至主要内容
临床试验/CTRI/2024/12/077700
CTRI/2024/12/077700尚未招募不适用

A clinical study to evaluate the effect of Trataka karma in Computer Vision Syndrome in Information Technology professionals: A Randomized Controlled Trial.

Dr Aishwarya Hariram Meshram1 个研究点 分布在 1 个国家目标入组 64 人开始时间: 2024年12月16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
64
试验地点
1
主要终点
To evaluate and compare the efficacy of Trataka karma in Computer Vision Syndrome based on Computer Vision Syndrome Questionnaire.

研究概览

简要总结

In the present study, total 64 participants will be taken for trial dividing them in 2 equal groups. Group A will receive the trial procedure ’Trataka karma’ and Group B will receive the already proven drug ’CMC 0.5% e/d’ Follow up will be taken on day- 0, 15 and 30. Result will be concluded based on assessment criteria.

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
20.00 Year(s) 至 40.00 Year(s)(—)
性别
All

入选标准

  • Patients working in IT sector with screen time more than 4 hours a day for 3 months with or without the use of any spectacles.
  • Patients of CVS evaluated by Computer Vision Syndrome Questionnaire with score more than or equal to 6 and Schirmers test with score less than 15.

排除标准

  • Known hypersensitivity to study medications and those who had used any other topical ophthalmic medications within 14 days (other than tear substitutes).
  • History of any active ocular infection or allergy or surgery within 12 months or use of any contact lenses.
  • Patients of Sjogren syndrome and other autoimmune diseases.
  • Any systemic diseases like uncontrolled HTN or DM or congenital deformities or thyroid abnormalities or renal diseases or cardiac diseases and carcinoma will be excluded.

结局指标

主要结局

To evaluate and compare the efficacy of Trataka karma in Computer Vision Syndrome based on Computer Vision Syndrome Questionnaire.

时间窗: Follow up will be taken on day 15 and 30.

次要结局

  • To evaluate & compare the efficacy of Trataka karma in Computer Vision Syndrome based on Schirmers test.(Follow up will be taken on day 15 & 30.)

研究者

发起方
Dr Aishwarya Hariram Meshram
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr Aishwarya Hariram Meshram

Guide

研究点 (1)

Loading locations...

相似试验