MedPath

Saptanna Ghrita and Shringaveradi Taila Nasya in Prathama Patalagata Timira (simple myopia)

Not yet recruiting
Conditions
Subjective visual disturbances. Ayurveda Condition: PRATHAMA-PATALAGATADOSHAH,
Registration Number
CTRI/2021/07/035155
Lead Sponsor
Gurukul campus UAU Haridwar
Brief Summary

This study is a open label, randomised parallel clinical trial to determine the Efficacy of Evaluation of Saptanna Ghrita and Shringaveradi Taila Nasya in Prathma Patalagata Timira in Simple Myopia for age group between 13 to 35 years daily for 45 days.The study will be conducted at Gurukul Campus UAU Haridwar in 40 patients.The assessment will be done on basis of  Subjective and Objective parameters. The study will be conducted at OPD/IPD level of PG Depatment of Shalakya Tantra.The assessment will be done at 1st,15th,30th and 45th day of the clinical trial and the results obtained will be tabulated and statistically analyzed using appropriate tests.

Detailed Description

Not available

Recruitment & Eligibility

Status
Not Yet Recruiting
Sex
All
Target Recruitment
40
Inclusion Criteria
  • 1)The patients presenting with features of Prathama patalagata Timira(Simple Myopia) 2)Vatika Timira 3)Those fit for Nasya 4)Patients having -0.25D to -2.5D of vision.
  • 5)Patients aged between 13 to 35 years.
Exclusion Criteria
  • 1)Dwitiya,tritiya and chaturtha patalagata timira.
  • 2)Paittik Timira, Shlaismik Timira, Raktaj Timira,Sannipataja Timira.
  • 3)High myopia or progressive myopia.
  • 4)Congenital myopia.
  • 5)Myopia with systemic disease like TB, Hypertension, DM etc.
  • 5)Patients more than -2.5D of vision.
  • 6)Hypermetropia,presbyopia and Astigmatism.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
2)Eye strain1st, 15th, 30th and 45th day.
4)Watering eyes1st, 15th, 30th and 45th day.
Relief in Subjective parameters like-1st, 15th, 30th and 45th day.
3)Headache1st, 15th, 30th and 45th day.
1)Avyaktha Darshana(Blurring of Vision)1st, 15th, 30th and 45th day.
Secondary Outcome Measures
NameTimeMethod
Assessment will be done on the basis of Visual acuity and Diopetric power.At 1st and 45th day.

Trial Locations

Locations (1)

U.A.U. Gurukul Campus, Haridwar

🇮🇳

Hardwar, UTTARANCHAL, India

U.A.U. Gurukul Campus, Haridwar
🇮🇳Hardwar, UTTARANCHAL, India
Sasmita Gumansingh
Principal investigator
9437317615
sasmitagumansingh@gmail.com

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.