Comparison of two different treatment regimens for treatment of leprosy.
Not Applicable
Completed
- Conditions
- Health Condition 1: A304- Borderline lepromatous leprosyHealth Condition 2: A303- Borderline leprosyHealth Condition 3: A302- Borderline tuberculoid leprosyHealth Condition 4: A300- Indeterminate leprosyHealth Condition 5: A305- Lepromatous leprosyHealth Condition 6: A309- Leprosy, unspecifiedHealth Condition 7: A308- Other forms of leprosyHealth Condition 8: A301- Tuberculoid leprosy
- Registration Number
- CTRI/2022/08/045078
- Lead Sponsor
- S Nijalingappa Medical College and HSK Hospital and Research centre
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 40
Inclusion Criteria
Patients of both genders who are newly diagnosed with leprosy and are willing for study
Exclusion Criteria
Patient below 5 years and above 90 years.
Patient refusal to give consent
Pregnant and lactating females.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Changes in clinical features, Dermoscopy changes would be checkedTimepoint: Every 4 weeks
- Secondary Outcome Measures
Name Time Method Changes in Histopathology would be checked.Timepoint: every 24 weeks