To find out and compare the effectiveness of Kanaka Taila and Kumkumadi Taila nasya in the treatment of Vyanga (a skin disorder )

Not Applicable

Not yet recruiting

• Conditions: Health Condition 1: L988- Other specified disorders of the skin and subcutaneous tissue

• Registration Number: CTRI/2020/04/024755
• Lead Sponsor: PDEAs College of Ayurveda and Research Centre Akurdi

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 24 November 2021

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

Patients having classical symptoms of vyanga like tanu niruja shyava mandal on face of patient arha for nasya

Exclusion Criteria

Known case of systemic diseases vyanga either congenital or along with kushta known case of inflammatory disease of nose

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
To evaluate the efficacy of kanaka tail nasya and kumkumadi tail nasya in the management of vyanga on the basis of subjective and objective parameters within 15 daysTimepoint: Daily assessment will be done for 7 days in the duration of nasya treatment and final assessment follow up will be done on 15th day with the window period of 5 days

Secondary Outcome Measures

Name	Time	Method
To study the adverse effects if anyTimepoint: For 7 days of nasya administration