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Effect Of Triphala Kwath Parisheka(Stye).

Not Applicable
Conditions
Health Condition 1: H000- Hordeolum (externum) (internum) ofeyelid
Registration Number
CTRI/2024/08/072323
Lead Sponsor
Dr Shivani Virkar
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Patient having sign and symptoms of Anjannamika .

Age group 15-60 years.

Selection of patient will be irrespective of Gender socioeconomic

status and religion.

Exclusion Criteria

Patients age below 15 years and above 60 years.

Patients who will not give written consent.

Patient having diseases like DM, HIV+ve, HbsAg, etc.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Reduction in signs and symptoms of Anjannamika (stye) after application of triphala kwath parishekaTimepoint: 7 days
Secondary Outcome Measures
NameTimeMethod
where the trial group (triphala kwath parisheka) stands in comparison with control group (haridradi parisheka) in reduction with the signs & symptoms of Anjannamika(stye).Timepoint: 18 months
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