To Evaluate The Effect Of Pratimarsha Nasya With Aschyotana In Comparison To Marsha Nasya With Tarpana In Pratham Patalgata Timira (Simple Myopia)
Trial Snapshot
- Phase
- Not Applicable
- Status
- Not yet recruiting
- Sponsor
- Enrollment
- 60
- Locations
- 1
- Primary Endpoint
- The improvement will be assessed on the basis of;
Study Overview
Brief Summary
This study is an open level randomized parallel arm clinical trial to determine the efficacy of pratimarsha nasya with aschyotan and marsha nasya with tarpana in pratham patalgata timira(Simple Myopia) for the age group between 8 to 40 years for 35 days. The study will be conducted at Uttrakhand Ayurveda University, Gurukul Campus, Haridwar on 60 patients. Assessment will be done on the basis of subjective and objective parameters. Study will be conducted at OPD/IPD level of PG department of Shalakya Tantra. Assessment will be done on 1st, 15th and 35th day of clinical trial and result obtained will be tabulated and statistically analyzed using appropriate tests.
Study Design
- Study Type
- Interventional
- Allocation
- Computer generated randomization
- Masking
- Open Label
Eligibility Criteria
- Ages
- 8.00 Year(s) to 40.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •Patient presenting with sign and symptoms of Pratham Patalgata Timira and Simple Myopia.
Exclusion Criteria
- •Dwitiya, Tritiya and Chaturtha Patalgata Timira
- •Congenital, Pathological and Functional Myopia
- •Other Refractive Errors (Hypermetropia, Astigmatism)
- •Presbyopia
- •Optical Correction >-3D
- •Patient with uncontrolled Hypertension, Diabetes
- •Unfit for Nasya.
Outcomes
Primary Outcomes
The improvement will be assessed on the basis of;
Time Frame: The assessment of patient will be done on 1st, 15th & 35th day
1. Subjective parameters- Avaykat Darshana(Blurred vision), Eye Strain, Watering of eyes, Headache
Time Frame: The assessment of patient will be done on 1st, 15th & 35th day
2. Objective parameters-
Time Frame: The assessment of patient will be done on 1st, 15th & 35th day
Visual Acuity, Dioptric power
Time Frame: The assessment of patient will be done on 1st, 15th & 35th day
Secondary Outcomes
- The improvement will be assessed on the basis of;(Eye Strain, Watering of eyes, Headache)