Application of Gomaya Siddha Taila Nasya in Prathamapatalagata Timir w.s.r to Simple Myopia.

Single arm clinical trail to assess the efficacy of Gomaya Siddha Taila Nasya in Prathamapatalagata Timir w.s.r to Simple Myopia. - NIL

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/03/083080

Enrollment

Registered

2025-03-21

Start date

Unknown

Completion date

Unknown

Last updated

2025-04-07

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: 1)Signs and symptoms of prathamapatalagata timir i.e. avyakta rupa . 2) Signs and symptoms of simple myopia i.e blurred vision headache, eye strain. 3) Fit for informed consent

Exclusion criteria

Exclusion criteria: 1) K/c/o Pathological myopia, high myopia with degenerative and gross retinal changes. 2) Myopia associated with neighbouring structural deformities like corneal opacity. 3) Patients suffering from any of the systemic disorders like DM, HTN. 4) Patients who have underwent any of the refractive surgeries. 5) Patients who are contraindicated for Nasya procedure. 6) Patients with myopia having allergy to cow dung smell or not willing to treat with gomaya medications.

Design outcomes

Primary

Measure	Time frame
Improvement in Vision .Timepoint: From 7-14 days after administration of nasya	—

Secondary

Measure	Time frame
Improvement in auto refractive index of eye.Timepoint: from 14-21 days after administration of nasya	—

Countries

India

Contacts

Public ContactDr Anil Deshmukh

SSTAC SANGAMNER

ranwaraanil@gmail.com9822262627

Outcome results