MedTrace Logo

A Comparative Study of Occlusive Heat Patch in the Treatment of Warts

NCT01746056 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 73

Last updated 2022-11-15

No results posted yet for this study

Summary

The goal of this study is to determine the safety and efficacy of the occlusive heat patch for the treatment of verrucae (warts).

Conditions

  • Verruca (Warts)

Interventions

DEVICE

Occlusive Heat Patch

The heat patch will be applied for 2 hours every day for a period of 12 weeks.

Sponsors & Collaborators

  • Ferndale Laboratories, Inc.

    collaborator INDUSTRY

  • Yale University

    lead OTHER

Principal Investigators

  • Richard Antaya, MD · Yale University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
5 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-12-31
Primary Completion
2019-10-11
Completion
2019-10-31

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01746056 on ClinicalTrials.gov