Sera application in leprosy patients
Not Applicable
Completed
- Conditions
- Health Condition 1: null- Dry eye patients of Hansens disease
- Registration Number
- CTRI/2013/07/003802
- Lead Sponsor
- Regional Institute of ophthalmology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 102
Inclusion Criteria
both sexes of patients of Hansen disease of age group 23yr to 75 yr were enrolled
Exclusion Criteria
Patients(both sexes) having active ocular and lid infection, active keartitis , lid deformity, history of punctual occlusion within last three months, pregnancy and lactation, were excluded from the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate comparative efficacy of topically applied 20% umbilical cord blood serum (UBS) and 20% autologous serum (ALS) with preservative free artificial tear drop (AT) in moderate to severe dry patients of Hansenâ??s disease along with change in tear protein profile.Timepoint: 21/04/2011
- Secondary Outcome Measures
Name Time Method nilTimepoint: none