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临床试验/CTRI/2025/02/081243
CTRI/2025/02/081243招募中2/3 期

A Randomized Clinical Trial To Evaluate The Efficacy Of Go-Ghrita Aschyotana With And Without Shadanga Guggulu Orally In The Management Of Shushkakshipaka W.S.R. To Computer Vision Syndrome(CVS)

Madan Mohan Malviya Government Ayurved College Udaipur Rajasthan1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年4月1日最近更新:

试验速览

阶段
2/3 期
状态
招募中
发起方
入组人数
60
试验地点
1
主要终点
Improvement in signs and symptoms of Shushkakshipaka w.s.r. to Computer Vision Syndrome(CVS) after treatment.

研究概览

简要总结

This is a clinical trial to compare efficacy of Go- Ghrita Aschyotana  and Shadanga Guggulu on Shushkakshipaka with special reference to Computer Vision Syndrome. In this trial 2 groups each of 30 patients will be selected. Group A will be administered with Go-Ghrita Ashchyotana and oral administration of Shadanga Guggulu Vati 2 BD with lukewarm water along with counseling for changing the working style and standard. Group B will be administered with Go-Ghrita Ashchyotana only.

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
18.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • Patients using computer or any visual display terminal at least 3 hours per day presenting with clinical features of 1.Netrayasa (Eye strain) 2.Avila Darshana (Blurred vision) 3.Shiro abhitapa (Headache) 4.Netra raga (conjunctival congestion) 5.Netra Daha (Burning sensation) 6.Vishushkatva (Dryness) 7.Slow refocusing 8.Excessive fatigue (Neck/Shoulder/Back pain).

排除标准

  • 1.Patients suffering from symptoms of dry eye due to causes other than excess exposure to visual display terminals.
  • 2.Patients suffering from systemic illness or taking medications which are known to affect tear quantity and quality.
  • 3.Complicated case with acute/chronic infective infections of lid, conjunctiva, cornea and sclera.

结局指标

主要结局

Improvement in signs and symptoms of Shushkakshipaka w.s.r. to Computer Vision Syndrome(CVS) after treatment.

时间窗: 30 days.

次要结局

  • Improvement in other associated symptoms.(15th day, 30th day)

研究者

发起方
Madan Mohan Malviya Government Ayurved College Udaipur Rajasthan
申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Dr Rishabh Sikarwal

Madan Mohan Malviya Government Ayurved College, Udaipur(313001), Rajasthan, India

研究点 (1)

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