CTRI/2019/07/020070Not yet recruitingNot Applicable
To Compare the efficacy and safety of Intradermal versus Intralesional Purified Protein Derivative (PPD) for treatment of Common warts in children
Himachal Pradesh University1 site in 1 country100 target enrollmentStarted: July 14, 2019Last updated:
Trial Snapshot
- Phase
- Not Applicable
- Status
- Not yet recruiting
- Sponsor
- Himachal Pradesh University
- Enrollment
- 100
- Locations
- 1
- Primary Endpoint
- Not yet recruiting
Study Overview
Brief Summary
I am going on intervention study include title to compare the efficacy and safety of Intradermal versus Intralesional Purified Protein Derivative (PPD) in treatment of Common warts in children.Dose schedule of PPD include 10TU per0.1 ml given intradermal and Intralesional at 2weekly interval upto 8weeks and asked patient to follow up at 12weeks to see resolution of warts.
Study Design
- Study Type
- Interventional
- Allocation
- Stratified randomization
- Masking
- Outcome Assessor Blinded
Eligibility Criteria
- Ages
- 5.00 Year(s) to 15.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •Children of age 5 to 15 years clinically diagnosed with common warts.
Exclusion Criteria
- •Patients with immune suppression from any disease or drug therapy.
Outcomes
Primary Outcomes
Not yet recruiting
Time Frame: Not yet recruiting
Secondary Outcomes
- NA(NA)
Investigators
Study Sites (1)
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