Study of blood letting using leech application in the patients suffering from keloid.
Phase 2
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2020/03/023674
- Lead Sponsor
- Dr Pankaj Dixit
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Diagnosed patients of keloids irrespective of age, sex size, and site.
Patients willing to participate and have given a writen consent for the same
Exclusion Criteria
Uncontrolled D.M.
ï?? Seropositive patients- HIV, HbsAg
ï?? Patients having deranged coagulation profile
ï?? Patients taking antiplatelet drugs
ï?? Infection of or near the keloid.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Relief in keloid using DLQI and POSAS scaleTimepoint: 8 weeks
- Secondary Outcome Measures
Name Time Method arresting the local spread of keloidTimepoint: 8 weeks