Skip to content

To Compare the efficacy of 20% Podophyllin and 100% Trichloroacetic acid in the treatment of anogenital warts

A Comparative study on the efficacy of 20% Podophyllin versus 100% Trichloroacetic acid in the treatment of anogenital warts - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/03/063810
Enrollment
50
Registered
2024-03-07
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-01

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

Conditions

Health Condition 1: B078- Other viral warts

Interventions

Intervention1: 20% Podophyllin: Patients in group A with anogenital wart will be treated with 20% podophyllin application weekly once for 6 weeks and followed up 2 weeks interval for another 6 weeks f

Sponsors

Dr S Ramya
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with anogenital warts willing to give written informed consent will be divided into group A and group B.25 Patients in group A will receive 20% podophyllin.25 Patients in group B will receive 100% TCA. Maximum 6 sittings will be given at weekly interval. Patients will receive no other therapies during the study. Patients will be advised partner screening and usage of barrier contraception during the study.

Exclusion criteria

Exclusion criteria: Before starting the study Pregnant and lactating women. During the study If patient develops severe side effects like ulceration / intolerant to pain during the treatment. If patient wants alternate treatment during the study. If patient wants to discontinue the treatment.

Design outcomes

Primary

MeasureTime frame
Clinical improvement or resolution of anogenital wartsTimepoint: 6 weeks

Secondary

MeasureTime frame
Disappearance or Recurrence of of anogenital wartsTimepoint: 12 weeks

Countries

India

Contacts

Public ContactDr S Ramya

Chengalpattu Medical College and Hospital

dermcliniccmch@gmail.com8110082516

Outcome results

None listed

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