Study of efficacy of Nishadi Ghana Vati and Karanja tail local application in skin disease

Phase 2

Not yet recruiting

• Conditions: Atopic dermatitis, unspecified,

• Registration Number: CTRI/2021/01/030491
• Lead Sponsor: Manisa Singh

Brief Summary

This study is Randomized, controlled clinical study of Nishadi Ghana Vati 500mg BD orally after meal with Karanja Tail local application for 30 days and follow up on 0th, 16th and 31th day.This study is conducted as PG course at single centre.The primary outcome is decrease in itching, pain, dryness of lesion and decrease in size of 1 or 2 large lesion

Detailed Description

Not available

Study Timeline

• Last Update Posted: 2021-01-14
• Study Start: 2021-01-20

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: All
• Target Recruitment: 33

Inclusion Criteria

The patient will be diagnosed on the basis of Symptoms of Vicharchika(Eczema) given in Sushruta Samhita a) Mandala (patches) b) Atikandu (severe itching) c) Ruja (pain) d) Rukshata (dryness) Patients who are co-operative and ready to give written consent Duration of symptoms is 1 year.

Exclusion Criteria

Patients having skin disorder other than eczema Eczema with systemic illness like severe DM, IHD Complicated or steroid dependent Eczema.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Decrease in itching, pain, dryness of lesion and decrease in size of 1 or 2 large lesions	30days

Secondary Outcome Measures

Name	Time	Method
Nishadi Ghana Vati orally with Karanja Tail local application is more effective than Arogyavardhini Vati orally with Karanja Tail local application	In 31 days

Trial Locations

Locations (1)

Government Ayurved Hospital, Vazirabad, Nanded; 🇮🇳 Nanded, MAHARASHTRA, India

Government Ayurved Hospital, Vazirabad, Nanded

🇮🇳Nanded, MAHARASHTRA, India

Manisa Singh

Principal investigator

8339065877

manisasingh688@gmail.com