Clinical study to Evaluate the efficacy of Triphaladhyaghrita Pratimarsha Nasya in Simple Myopia

Phase 2

Not yet recruiting

• Conditions: Myopia. Ayurveda Condition: TIMIRAH,

• Registration Number: CTRI/2023/03/050822
• Lead Sponsor: Dr Poonam Gajanan Belgaonkar

Brief Summary

This study is single blind randomized controlled clinical study to evaluate the efficacy of Triphaladhya ghrita pratimarsha nasya in simple myopia.

Total 200 patients of age 8 to 30 years of both sex will be randomly selected for this trial and divided in to two groups.

Group A Treated with Triphaladhya ghrita pratimarsha nasya

Adult dose (16 to 30 years) two drops in each nostril morning and evening for 90 days.

Child dose (8 to 15 years) One drop is each nostril morning and evening for 90 days.

Group  B – Treated with Abhijeet Taila Pratimarsha Nasya

Adult dose (16 to 30 years) two drops in each nostril morning and evening for 90 days.

Child dose (8 to 15 years) One drop is each nostril morning and evening for 90 days.

Data will be analysed and appropriate statistical tests will be applied.

Detailed Description

Not available

Study Timeline

• Study Start: 2023-04-25
• Last Update Posted: 2023-08-03

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: All
• Target Recruitment: 200

Inclusion Criteria

patients of simple myopia with low error less than or equal to minus 3D with normal opthalmoscopic findings.

Exclusion Criteria

patients of moderate myopia minus 3D to minus 6D Patients of High myopia greater than or equal to minus 6D Keratometry Reading less than 40D And greater than 45D Compound myopia and astigmatism excluded axial length greater than 28 excluded patient with other ocular pathology involving glaucoma cataract retinopathy corneal ulcer conjunctivitis uveitis excluded.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
efficacy of Triphaladhyaghrita pratimarsha nasya in simple myopia	90days

Secondary Outcome Measures

Name	Time	Method
Adverse Reaction if any	90days

Trial Locations

Locations (1)

Seth Tarachand Ramanath Charitable Ayurvedic hospitl; 🇮🇳 Pune, MAHARASHTRA, India

Seth Tarachand Ramanath Charitable Ayurvedic hospitl

🇮🇳Pune, MAHARASHTRA, India

DrPOONAM GAJANAN BELGAONKAR

Principal investigator

8605657046

dr.poonam2785@gmail.com