A clinical study to see the effect of some Ayurvedic formulation in the treatment of far sightedness.

Phase 2

Completed

• Conditions: Health Condition 1: H520- Hypermetropia

• Registration Number: CTRI/2021/12/038889
• Lead Sponsor: Sane Guruji Arogya Kendra

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2023-12-21
• Last Update Posted: 1 April 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 56

Inclusion Criteria

1. Patients having symptoms of Prathama Dwitiya Patalgata Timir will be included.

2. Patients who have = +5 D in both the eyes

3. The patient age from 18 years to 60 years of age

4. Patient having vision of 6/9 or less i.e., 6/12, 6/18,6/24, 6/36, 6/60.

5. Patient yogya for Nasya Karma.

6. Patient of either gender will be included in the study.

Exclusion Criteria

1. Patients having symptoms of Tritiya and Chaturtha Patalgata Timir will be excluded like Kacha and Linganasha.

2. Patient suffering from infectious disease e.g.-viral, bacterial or fungal conjunctivitis, blepharitis and trachoma.

3. Patient having known case of Hypertension, HIV, TB, Rheumatic Heart Disease, Bronchial Asthma, Thyroid disorder.

4. Hypermetropia associated with other ocular disease such as cataract, glaucoma, retinal disease, chorioretinitis, iridocyclitis, choroidal disease, vitreal opacity, cornel opacity, corneal ulcer.

5. Congenital, Acquired non physiological hypermetropia like index hyermetropia, pseudophakic hypermetropia.

6. Refractive errors like astigmatism, myopia, presbyopia and other ocular pathologies will be excluded.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
A clinical study to evaluate efficacy of Bhaskar Ghrita Nasya and Saptamrita Lauha Vati in Prathama and Dwitiya Patalgata Timir w.r.t Hypermetropia. Parameter of efficacy will be visual acuity before and after treatmentTimepoint: Follow up will betaken on 1st, 11th and 21st day. Parameter of efficacy will be visual acuity before and after treatment

Secondary Outcome Measures

Name	Time	Method
A comparison between efficacy of Bhaskar Ghrita Nasya with Saptamrita Lauha and Saptamrita Lauha alone in Prathama and Dwitiya Patalgata Timir w.r.t HypermetropiaTimepoint: Total duration of the study will 18 months.