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Clinical Trials/CTRI/2025/03/082984
CTRI/2025/03/082984Not yet recruitingNot Applicable

Combined effect of rasna dasamoola ghritha internally and netra abhyangam with ksheerabala taila (7 avarti) in myopic astigmatism in the age group of 5-16 years

Anagha T1 site in 1 country34 target enrollmentStarted: April 1, 2025Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
34
Locations
1
Primary Endpoint
Improvement of unaided and aided visual acuity in patients with

Study Overview

Brief Summary

Astigmatism is a common refractive error which causes blurry vision. Myopic astigmatism comes under refractive type of regular astigmatism. Asthenopia, defective vision and distortion of objects are the common symptoms of astigmatism. Conventional treatment methods include wearing corrective lenses or refractive surgery. Refractive errors are included under Timira roga in Ayurveda classics. The symptoms of myopic astigmatism bear resemblance to those of Prathama patala gata vatika timira. Acharya Vagbhata mentioned Snehapana initially while explaining Timira chikitsa. In the outpatient treatment, use of Rasna dasamoola ghritha internally and netra abhyanga with Ksheerabala taila (7 avarti) is found to yield positive results in patients with myopic astigmatism. Rasna dasamoola ghritha is a formulation containing drugs mainly of vatahara and brimhana properties. Ksheerabala taila is having rasayana and indriya prasadana action. Therefore, the study is planned to assess the combined action of Rasnadasamoola ghritha internally and netra abhyangam with Ksheerabala taila (7 avarti) in myopic astigmatism. The study is designed as a pre and post interventional study with a sample size of 34 participants in the age group of 5 to 16 years irrespective of gender from the outpatient department of Shalakyatantra, Govt. Ayurveda College Hospital, Kannur. The intervention will be given for 30 days. Changes in visual acuity from baseline will be assessed on 15th , 31st , 46th and 61st day and changes in refraction on 31st day and 61st day.

Study Design

Study Type
Interventional
Allocation
Na
Masking
None

Eligibility Criteria

Ages
5.00 Year(s) to 16.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • Participants with best corrected visual acuity greater than or equal to 0.18 in LogMar visual acuity chart.
  • Participants who are willing to give an informed verbal or written assent and parents consent.

Exclusion Criteria

  • Participants with previous ocular surgery or trauma.
  • Participants with any other ocular pathologies.
  • Participants with mandagni.

Outcomes

Primary Outcomes

Improvement of unaided and aided visual acuity in patients with

Time Frame: Visual acuity assessment will be done on 0th, 15th | , 31st, 46th and 61st day of treatment.

myopic astigmatism using LogMar visual acuity chart.

Time Frame: Visual acuity assessment will be done on 0th, 15th | , 31st, 46th and 61st day of treatment.

Secondary Outcomes

  • Improvement dioptric power of eyes in patients with myopic(astigmatism using retinoscope, autorefractometer and subjective method of)

Investigators

Sponsor
Anagha T
Sponsor Class
Other [self]
Responsible Party
Principal Investigator
Principal Investigator

Anagha T

Government Ayurveda College, Kannur

Study Sites (1)

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