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To see the efficacy of bakuchi compound and khadira kwatha with and without virechana karma in the the management of shwitra(Vitiligo).

Phase 2
Completed
Conditions
Health Condition 1: L80- Vitiligo
Registration Number
CTRI/2019/05/019012
Lead Sponsor
ational Institute of Ayurveda
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
28
Inclusion Criteria

1.Patients in the age group of 18 to 60 years of either sex.

2.Patient diagnosed as shwitra (vitiligo) on the basis of clinical features mentioned in Ayurveda texts.

3.Patients fit for virechana.

4.Patient with history of shwitra less than or equal to five years.

5.Patient willing to participate in the clinical trial.

Exclusion Criteria

1.Patient with age group of less than 18 years and more than 60 years.

2.White anesthetic spots, which are characteristic of leprosy.

3.Patches in genital areawill be excluded from the study.

4.Vitiligo patches complicated with eczema.

5.Patients with evidence of malignancy, diabetes mellitus with complication, albinism.

6.Pregnant women and lactating mother.

7.Patient participated in any clinical trial within last six months.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Primary outcome: Assessment of changes in specific signs and symptoms of shwitra <br/ ><br>Secondary outcome: Any adverse effect in the values of haematological test and in clinical signs and symptoms.Timepoint: 60 days
Secondary Outcome Measures
NameTimeMethod
Any adverse effect in the values of haematological test and in clinical signs and symptoms.Timepoint: 60 days
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