A clinical trial to study the efficacy of Ilaguseena chooranam for Venpadai
- Conditions
- Health Condition 1: null- patients suffering from venpadaiHealth Condition 2: L80- Vitiligo
- Registration Number
- CTRI/2018/08/015453
- Lead Sponsor
- S karthika
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Hypo pigmented patches with hyper pigmented border without any structural changes in any part of the body. vitiligo present any part of the body.Patients who are willing to stay in IPD Ward for 27 days or willing to attend OPD. Children who are willing to undergo investigation and give blood and urine samples for laboratory investigation. Patientâ??s informant / Parent willing to sign the informed consent stating that he/she will consciously stick to the treatment during 27 days but can opt out of the trial of his / her own conscious discretion.
Albinism
Dermatological aspect of leprosy
Tinea versicolor
Burn scars
Dermatological aspect of addisons diseases
Post inflammatory hypopigmentation
Pityriasis alba
Alopecia aerate
chemical leucoderma
white patches on mucous membrane
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The Therapeutic Efficacy of Trial drug Ilaguseena Chooranam on Venpadai <br/ ><br>Timepoint: 27 days
- Secondary Outcome Measures
Name Time Method Evaluation of Siddha Diagnostic ParametersTimepoint: 27 days