CTRI/2023/02/049750
Not yet recruiting
Phase 2
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
ConditionsHealth Condition 1: H524- Presbyopia
Overview
- Phase
- Phase 2
- Intervention
- Not specified
- Conditions
- Health Condition 1: H524- Presbyopia
- Sponsor
- ational Institute of Ayurveda
- Status
- Not yet recruiting
- Last Updated
- 3 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •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)
Exclusion Criteria
- •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.
Outcomes
Primary Outcomes
Not specified
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