To see the effect of Aragvadha Patra Lepa and Aragvadha Kashaya in Eczema

Phase 1/2

Not yet recruiting

• Conditions: Dermatitis, unspecified. Ayurveda Condition: VICARCIKA,

• Registration Number: CTRI/2023/07/055044
• Lead Sponsor: Uttarakhand Ayurved University

Brief Summary

This study is an open label randomized clinical trial to see the clinical effect of Aragvadha patra lepa with Aragvadh Kashaya in Vicharchika. In this trial, patients with classical symptoms of vicharhika will be selected from OPD and IPD of Kayachikitsa department of Rishikul campus Uttarakhand Ayurved University Haridwar. In this study, 30 patients will be selected and will be given Aragvadha Kashaya orally and Aragvadha patra lepa for external application for 30 days. Assessment will be done on the basis of various parameters as before and after the treatment is done.

Detailed Description

Not available

Study Timeline

• Last Update Posted: 2023-07-07
• Study Start: 2023-07-19

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

• 1. Age group between 20 to 60 years. 2. Classical symptoms of Vicharchika like.
• 3. Kandu (itching), Pidika (eruption), Vaivarnyata (discoloration), Daha (burning sensation),Rukshata( dryness) Vedana( pain). 4. Patient willing to participate in above mentioned trial with informed consent.

Exclusion Criteria

• Age group less than 20 year and more than 60 year.
• Pregnant and lactating women.
• Patient with other cutaneous symptoms of psoriasis, leprosy, local burn etc.
• Any other secondary skin diseases.
• Uncontrolled diabetic patients.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Subjective parameters	0,10,20,30,45 days
2. Daha (burning sensation )	0,10,20,30,45 days
4. Vaivarnyata (Discoloration)	0,10,20,30,45 days
1. Kandu (itching)	0,10,20,30,45 days
3. Vedana (Pain)	0,10,20,30,45 days
5. Pidika (Eruption)	0,10,20,30,45 days
6. Rukshata (Dryness)	0,10,20,30,45 days

Secondary Outcome Measures

Name	Time	Method
Onjective parameters	1. No. of lesion

Trial Locations

Locations (1)

Rishikul Campus Haridwar; 🇮🇳 Hardwar, UTTARANCHAL, India

Rishikul Campus Haridwar

🇮🇳Hardwar, UTTARANCHAL, India

Manisha Bisht

Principal investigator

8126215792

manishabisht57@gmail.com