Unhealthy diet as a cause in development of skin disease and its treatment with some Ayurvedic drugs

Phase 3

Completed

• Conditions: Dermatitis, unspecified, having sign and symptoms of vicharchika kustha,

• Registration Number: CTRI/2016/08/007192
• Lead Sponsor: National Institute of Ayurveda

Brief Summary

A randomised clinical trial has been designed to assess the efficacy of *Trivá¹›ta CÅ«rṇa* with *Ä€ragvadha Patra* *Lepa* *&* *Ä€ragvadha Patra Lepa* alonein the management of *VicarcikÄ* (Eczema) 63 patients of*VicarcikÄ Kuṣṭha* were selected from O.P.D. of *RoganidÄna* evam *Viká¹›ti VijñÄna* department of N.I.A. and randomly taken in 2 groups, out of which 60 patients (30 patients each) were completed the trial treatment. Group A received *Trivá¹›ta CÅ«rṇa* with *Ä€ragvadha Patra* *Lepa* *&* Group B received *Ä€ragvadha Patra Lepa* alone for 4 weeks. All calculations were calculated through ‘Graph Pad In stat 3’ software. *Nitya* *Virecana* (Regular purgation) by *Trivá¹›ta* along with *Ä€ragvadha Patra Lepa* (Group A)proved more effective to control *Kaṇá¸Å«, SrÄva, DÄha, Piá¸Ä«kÄ, Vaivarṇya*, *RujÄ* & *Åšotha.* The synergistic actions of *Trivá¹›ta* along with *Ä€ragvadha Patra Lepa* are likely to check the etio-pathogenesis of *VicarcikÄ Kuṣṭha* (Eczema) and arrest its progress.**xml:namespace prefix = "o" ns = "urn:schemas-microsoft-com:office:office" /**

Detailed Description

Not available

Study Timeline

• Study Start: 2013-01-13
• Study Completion: 2014-09-21
• Last Update Posted: 2019-11-19

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

Patient with the classical sign and symptoms of VicarcikÄ Kuṣṭha viz Kaṇá¸Å« RujÄ Piá¸ikÄ SrÄva Ruká¹£atÄ ÅšyÄva DÄha RÄjÄ« Patients above 18 years and below 70 years of age Patients belonging to either gender.

Exclusion Criteria

The patient suffering from systemic disorders The pregnant women and lactating mother Patient less than 18 years and above 70 yrs of age.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Developed Dietetic guidelines for the patients of Kustharoga and ointment formulation for these kind of patient	follow up at every 15 days total duration 1 month

Secondary Outcome Measures

Name	Time	Method
Devoloped patient awareness about faulty dietary habits	1 month

Trial Locations

Locations (1)

National Institute of Ayurveda Jaipur; 🇮🇳 Jaipur, RAJASTHAN, India

National Institute of Ayurveda Jaipur

🇮🇳Jaipur, RAJASTHAN, India

Manisha Talekar

Principal investigator

8824854303

dr.mani21jan@gmail.com