A Randomized Clinical Trial to Evaluate the Efficacy of Ayurvedic Compound in Shushkakshipaka w.s.r. to Computer and Visual Display Terminal Vision Syndrome (CVDTS)

National Institute of Ayurveda1 个研究点分布在 1 个国家目标入组 60 人开始时间: 2020年2月11日最近更新: 2020年10月23日

试验速览

阶段: 2 期
状态: 尚未招募
发起方: National Institute of Ayurveda
入组人数: 60
试验地点: 1
主要终点: Evaluate the efficacy of Ayurvedic compound in computer and visual display terminal vision syndrome (CVDTS) W.S.R. to Shushkakshipaka

研究概览研究设计入排标准结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

Purpose- To Evaluate the Efficacy of Ayurvedic Compound in Shushkakshipaka w.s.r. to Computer andVisual Display Terminal Vision Syndrome (CVDTS)

GROUP A: Tarpana with Chakshushya**Ghrita and oraladministration of Shadanga Guggulu Vati

GROUP B: oral administration of Shadanga Guggulu Vati

研究设计

研究类型: Interventional
分配方式: Computer generated randomization
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

•Patients using computer at least 3 hours per day presenting with clinical features of
•Netrayasa (Eye strain)
•Avila Darshana (Blurred vision)
•Shiro abhitapa (Headache)
•Netra raga (conjunctival congestion)
•NetraDaha (Burning sensation)
•Vishushkatva (Dryness)
•Slow refocusing
•Excessive fatigue (Neck/Shoulder/Back pain).

排除标准

•1.Patient not willing for registration.
•2.Patients suffering from symptoms of dry eye due to causes other than excess exposure to visual display terminals.
•3.Patients suffering from systemic illness or taking medications which are known to affect tear quantity and quality.
•4.Complicated case with acute/chronic infective infections of lid, conjunctiva, cornea and sclera.

结局指标

主要结局

Evaluate the efficacy of Ayurvedic compound in computer and visual display terminal vision syndrome (CVDTS) W.S.R. to Shushkakshipaka

时间窗: 45 Days

次要结局

Any adverse event reported voluntarily, observed or enquire(45 Days)

研究者

发起方

National Institute of Ayurveda

申办方类型

Research institution and hospital

研究点 (1)

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