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NCT00328991 · ClinicalTrials.gov registry record · NA

Clinical Trial Evaluating Efficacy of Duct Tape for Treatment of Warts

A NA study, sponsored by Minneapolis Veterans Affairs Medical Center.

Completed
Registry status
NA
Development phase
90
Enrollment target

NCT00328991: Completed NA study, sponsored by Minneapolis Veterans Affairs Medical Center.

NCT00328991 is a NA study that has completed, run by Minneapolis Veterans Affairs Medical Center. The registered enrollment target is 90 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (94% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00328991, a NA study, has completed, sponsored by Minneapolis Veterans Affairs Medical Center.

COMPLETED
Registry status
NA
Development phase
90 participants
Enrollment target

Study Summary

This study is a double-blinded, controlled clinical intervention trial to evaluate the efficacy of duct tape occlusions therapy for the treatment of common warts. 80 patients completed this study, and were randomized 1:1 to receive pads which contained either moleskin+transparent duct tape or moleskin alone. The patients wore the pad over the target wart for 7 days at a time, removed the pad on the evening of the 7th day, and replaced the pad on the 8th day. This cycle was repeated for 8 weeks or until the wart resolved. The hypothesis was that duct tape occlusion therapy would be more therapeutic than moleskin for the treatment of the common wart. However, in our study there was only 21% resolution rate in the duct tape arm vs. 22% in the control group.

Interventions

  • DEVICE duct tape occlusion therapy

Trial Details

FieldValue
Enrollment Target 90 participants
Start Date 2004-10
Est. Completion 2005-12
Phase NA

What the finished NCT00328991 record still lists

NCT00328991 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 90 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (94% lower).

The record links to 0 conditions, and to 1 intervention - of which duct tape occlusion therapy is the first listed.

NCT00328991 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00328991 about?

NCT00328991 is a clinical study titled "Clinical Trial Evaluating Efficacy of Duct Tape for Treatment of Warts". This study is a double-blinded, controlled clinical intervention trial to evaluate the efficacy of duct tape occlusions therapy for the treatment of common warts. 80 patients completed this study, and were randomized 1:1 to receive pads which contained either moleskin+transparent duct tape or molesk...

What is the current status of trial NCT00328991?

This trial is currently completed. It is a NA study. The enrollment target is 90 participants. The study started on 2004-10. Estimated completion is 2005-12.

What interventions are being tested in trial NCT00328991?

The interventions under investigation include: duct tape occlusion therapy (DEVICE).

Who is sponsoring clinical trial NCT00328991?

This trial is sponsored by Minneapolis Veterans Affairs Medical Center, which has 28 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00328991's enrollment target sits among peer trials

90 941st of 2000 higher than 1,029 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00328991, the US trial registry maintained by the National Library of Medicine. NCT00328991 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.