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A TRIAL FOR COMPARING CLINICAl AND BIOPSY CHANGES OF NEEDLING VERSUS PLATELET RICH PLASMA IN EXTRAGENITAL CUTANEOUS WARTS

CLINICAL AND HISTOLOGICAL COMPARISON OF NEEDLING VERSUS INTRALESIONAL PLATELET RICH PLASMA IN EXTRAGENITAL CUTANEOUS WARTS: A RANDOMIZED CLINICAL TRIAL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/04/041988
Enrollment
70
Registered
2022-04-20
Start date
Unknown
Completion date
Unknown
Last updated
2022-05-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: B079- Viral wart, unspecified

Interventions

Intervention1: INTRALESIONAL PLATELET RICH PLASMA: INTRALESIONAL PLATELET RICH PLASMA USING 31G INSULIN SYRINGE AND KEEPING NUMBER OF PRICKS CONSTANT AT 10-12 PRICKS PER CENTIMETER SQUARE.INTERVENTION

Sponsors

RESEARCH CELL ALL INDIA INSTITUTE OF MEDICAL SCIENCES JODHPUR
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients who give informed written consent and fulfilling all the following criteria will be included in the study 1.Patients aged more than twelve years and less than sixty years 2. Patients having extragenital cutaneous warts. 3. Treatment wash-off period of at least 2 weeks for topical therapy and 4 weeks for systemic therapy.

Exclusion criteria

Exclusion criteria: Patient having any of the following criteria will be excluded from the study. 1. Inflamed or ulcerated warts 2. Patient on immunosuppressant drugs 3. Chronic kidney disease, Chronic liver disease, Uncontrolled Diabetes, Uncontrolled hypertension, Coagulopathy, Thrombocytopenia. 4. HIV, Hep B, Hep C 5. Advanced stage of internal malignancy

Design outcomes

Primary

MeasureTime frame
1.Investigator global assessment (Grade -1 to 5)/ Photographic assessment 2. Lesion count 3. Patient global assessment (VAS score)Timepoint: 4,8,12,16,2O WEEEKS

Secondary

MeasureTime frame
1. Quality of life assessment using Dermatology Life Quality Index -WARTS 2. Recording of side effects, if any, as per proforma 3. Histopathology slide viewing and counting of T cells in infiltrateTimepoint: DLQI AT BASELINE AND 12 WEEKS. BIOPSY AT BASELINE AND AT 12 WEEKS(FOR NON RESOLVING LESIONS), AND BASELINE AND ANYTIME AFTER BASELINE (FOR RESOLVING LESIONS)

Countries

India

Contacts

Public ContactDR SHUBHAM KUMAR

AIIMS JODHPUR

saurabhdoc@yahoo.co.in9968024250

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026