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

Randomized Control Clinical Study To Evaluate The Efficacy of Triphaladhyaghrita Pratimarsh Nasya in Simple Myopia

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2023/03/050822

Enrollment

200

Registered

2023-03-17

Start date

Unknown

Completion date

Unknown

Last updated

2023-04-03

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

Conditions

Health Condition 1: H521- Myopia

Interventions

None listed

Eligibility

Inclusion criteria

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

Exclusion criteria

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

Design outcomes

Primary

Measure	Time frame
efficacy of Triphaladhyaghrita pratimarsha nasya in simple myopiaTimepoint: 90days	—

Secondary

Measure	Time frame
Adverse Reaction if anyTimepoint: 90days	—

Countries

India

Contacts

Public ContactDr Poonam Gajanan Belgaonkar

Tilak Ayurved Mahavidyalaya Pune

salvisangeeta@yahoo.co.in09822082795

Outcome results