Effect of Jalauka-Avcharan and Vidangadi Lepa in the management of Dadru (Dermatophytosis).

Phase 3

Not yet recruiting

• Conditions: Other specified local infections of the skin and subcutaneous tissue. Ayurveda Condition: DADRU-KUSHTHAH,

• Registration Number: CTRI/2023/07/054869
• Lead Sponsor: Government PG Ayurveda College and Hospital Varanasi Uttar Pradesh India

Brief Summary

This study is an Interventional Open and Randomized group trial study, named- A COMPARATIVE CLINICAL STUDY OF JALAUKA-AVCHARAN AND VIDANGADI LEPA IN THE MANAGEMENT OF DADRU (DERMATOPHYTOSIS).

A total number of 60 patients suffering from dadru will be randomly selected from OPD and IPD of Government PG Ayurveda College and Hospital, Varanasi and will be divided into three groups, each group having 20 patients.

Group A- 20 patients will be treated with RAKTAMOKSHAN with the help of Jalauka of duration 17 days in three sittings.

Group B- 20 patients will be treated with Vidangadi Lepa of duration 17 days.

Group c- 20 patients will be given combined treatment of raktamokshan by jalauka along with Vidangadi Lepa of duration 17 days.

Follow up- After completion of treatment course of 17 days, there will be three follow ups at the interval of seven days.

First Follow up-      At 7th day

Second Follow up- At 14th day

Third Follow up-     At 21st day

Detailed Description

Not available

Study Timeline

• Study Start: 2023-07-25
• Last Update Posted: 2024-10-24

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

1 Patients are selected irrespective of sex occupation caste etc 2 Patients between age group 16 to 70 years are included in the study 3 Patients with classical sign and symptoms of Dadru will be taken 4 Patients having Hb value within normal range more than 10 mg per dl.

Exclusion Criteria

1 Patient of age group less than 16 and and more than 70 years 2 Patient who lies in the criteria of Raktamokshan Ayogya 3 Patients having Hb below 10mg per dl 4 Immuno-compromised patient Uncontrolled Diabetes Skin Cancer etc 5 Any haemorrhagic disorder or hereditary conditions Thallesemia Sickle cell anemia etc 6 Pregnant and Lactating mothers.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Relief in redness & Itching	10 days

Secondary Outcome Measures

Name	Time	Method
Reduction in lesion size	17 days

Trial Locations

Locations (1)

Government PG Ayurveda College and Hospital Varanasi 221002 UP; 🇮🇳 Varanasi, UTTAR PRADESH, India

Government PG Ayurveda College and Hospital Varanasi 221002 UP

🇮🇳Varanasi, UTTAR PRADESH, India

Dr Neha Bisht

Principal investigator

8273321161

nee8273@gmail.com