A clinical study to see the effect of some Ayurvedic formulation in the form of nasal administration in the treatment of simple myopia.

Phase 2/3

Completed

• Conditions: Myopia,

• Registration Number: CTRI/2020/11/029057
• Lead Sponsor: Sane Guruji Arogya Kendra

Brief Summary

This study is open labelled randomized comparative clinical trial to evaluate the effect of Bhringaraja Taila Nasya daily in the morning for 21 days in comparison with Abhijit Taila Nasya daily in the morning for 21 days in patients affected with Prathama and Dwitiya Patalagata Timir w.r.t Simple Myopia. The Primary outcome will be effect of Bhringaraja Taila Nasya on visual acuity and the secondary outcome will be comparison between the effect of trial drug and control drug in management of Prathama and Dwitiya Patalagata Timir w.r.t Simple Myopia.

Detailed Description

Not available

Study Timeline

• Study Start: 2021-01-03
• Study Completion: 2022-08-26
• Last Update Posted: 2023-03-29

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 80

Inclusion Criteria

• 1. Patient having signs and symptoms of Prathama and Dwitiya Patalagata Timir a will be included i.e blurriness, difficult to distant vision, visual hallucination.
• 2. The patient of age from 19 to 40 years,irrespective of gender 3) Patient who have low myopia 3D in both eyes.
• 4)Patients having a vision 6/9 or less i.e. 6/12, 6/18, 6/24, 6/36, 6/60 5) Patient yogya for Nasya karma.

Exclusion Criteria

• 1. Know case of Myopia associated with other ocular diseases such as Cataract glaucoma, Retinal diseases, Iridocyclitis, Vitreous opacity, Chorioretinitis.
• 2. Know case of Congenital Myopia, Pathological Myopia and other types of Myopia.
• 3. Patients suffering from infectious diseases e.g. bacterial,viral or Fungalconjunctivitis, Blepharitis, Tubercular infection.
• 4. Refractive errors like Hypermetropia, Astigmatism.
• 5. Patients having refractive error more than -3D in both eyes 6) Patients having known case of Diabetes Mellitus, Hypertension, HIV,HBSAg Tuberculosis, Thyroid disorder.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
A clinical study to evaluate efficacy of Bhingaraja Taila Nasya in Prathama and Dwitiya Patalgata Timir w.r.t Simple Myopia. Parameter of efficacy will be visual acuity before and after treatment	Duration of therapy is 3 weeks for each patient and the total duration of trial is 18 month

Secondary Outcome Measures

Name	Time	Method
comparison between efficacy	of Bhringaraja Taila Nasya and Abhijit Taila Nasya in

Trial Locations

Locations (1)

Sane Guruji Hospital; 🇮🇳 Pune, MAHARASHTRA, India

Sane Guruji Hospital

🇮🇳Pune, MAHARASHTRA, India

Vd Sneha Suryakant Air

Principal investigator

8379999327

snehaair2912@gmail.com