A Randomised Controlled Trial to assess the Efficacy of Jeevantyadi Ghrita Aschyotana and Jeevantyadi Ghrita oral Intake in the Management of Timira w.s.r to Presbyopia

ational Institute of Ayurveda0 个研究点目标入组 0 人开始时间: 待定最近更新: 2023年3月6日

试验速览

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•Patients willing to participate in the trial by taking written informed consent.
•Patients who are 35 years of age and from either sex.
•Patients having specific symptoms of prathama and dwitiya patalagata timira.
•Early to moderate presbyopia determined by screening monocular best-corrected distant visual acuity (VA)

•Patient with any active ocular infection.
•Patients with preauricular lymphadenopathy.
•Patients with moderate to severe dry eye .
•Patients with any abnormal lens findings.
•Patients having intraocular pressure (IOP) that is less than 5 millimeters of mercury (mmHg) or greater than 22 mmHg in either eye.
•prior diagnosis of ocular hypertension or glaucoma or currently being treated with any type of topical IOP lowering (glaucoma) medication
•Patients who have abnormal findings on dilated fundus examination in either eye.
•Patients having known history of retinal detachment or clinically significant retinal disease in either eye.
•Patients who have had surgical intervention (ocular or systemic) within 6 months prior to visit.
•Patients with severe systemic illnesses.
•Planned intra ocular or extra ocular surgery in either eye during study period

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