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A study to compare the effect of Triphaladi Ghrita Abhyantarpana along with spectacles and spectacles alone in improving age related difficulty in near vision (Presbyopia)

A Randomized Controlled Clinical Trial to Compare the Effectiveness of Triphaladi Ghrita Abhyantarpana along with Spectacle Correction and Spectacle Correction alone in Dwitiya Patalgata Timira (Presbyopia) - NA

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/10/096372
Enrollment
70
Registered
2025-10-23
Start date
Unknown
Completion date
Unknown
Last updated
2025-11-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: H524- Presbyopia

Interventions

None listed

Sponsors

Dr Deepali Rajesh Khedkar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patient aged between 35 to 50 years of age. 2.Near vision less than N 6 with normal distant vision i.e.6/6 vision. 3.Patients with clinical symptoms of presbyopia like Vivhal Darshan(Blurring of vision),Suchipasham na pashyati(Patient cannot thread a needle even with great efforts),Sukshma Cha Nekshate(Unable to locate fine objects),Netrayasa(Eyestrain),Shirobhitapa(Headache)

Exclusion criteria

Exclusion criteria: 1.Presbyopia associated with corneal degenerations,corneal ulcers,optic disc atrophy. 2.Presbyopia with cataract. 3.Psychiatric disorders,Metabolic disorders.

Design outcomes

Primary

MeasureTime frame
To study the changes in symptoms of Dwitiya Patalgata Timira (Presbyopia) like Vivhal Darshan(Blurring of vision), Suchipasham Na Pashyati(Patient cannot thread a needle even with great efforts), Sukshma Cha Nekshate(Unable to locate fine objects), Netrayasa(Eyestrain), Shirobhitapa(Headache)in both groups.Timepoint: Follow up for visual assessment will be done on 0th day, 7th day, 14th day, 30th day, 60th day spectacle correction will given on 60th day.

Secondary

MeasureTime frame
1.To study the changes in near point of accommodation with RAF rule in both groups. 2.To study the changes in axial length of eyeball with A scan in both groups.Timepoint: Follow up for visual assessment will be done on 0th day, 7th day,14th day, 30th day, 60th day.

Countries

India

Contacts

Public ContactDr Nutan Radaye

Dr. G. D. Pol Foundation YMT Ayurvedic Medical College

nutan.radaye.nr@gmail.com9820512695

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026