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NCT05070754 · ClinicalTrials.gov registry record · Phase 4

Cold Atmospheric Plasma Device for Pediatric Molluscum and Verruca

A Phase 4 study, sponsored by Medical University of South Carolina.

Completed
Registry status
Phase 4
Development phase
17
Enrollment target

NCT05070754 is a Phase 4 study that has completed, run by Medical University of South Carolina. The registered enrollment target is 17 participants.

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The verdict

NCT05070754, a Phase 4 study, has completed, sponsored by Medical University of South Carolina.

COMPLETED
Registry status
Phase 4
Development phase
17 participants
Enrollment target

Study Summary

This study is going to test a cold atmospheric plasma device (CAP), in particular a floating electrode-dielectric barrier device (FE-DBD), to treat warts and molluscum. The treatment device in this study generates cold atmospheric plasma (gaseous ionized molecules) to rid the virus from the body. Based on the successes of previous dermatologic studies, FE-DBD is being tested for this study to treat warts and molluscum. Patients will be enrolled to test the efficacy and safety of this device. The duration of the study is 4-12 weeks depending on treatment clearance. The number of lesions will be chosen by the dermatologist. Patients will receive standard of care therapy and/or NTAP depending on the number of lesions.

Interventions

  • DEVICE Cryotherapy
  • DEVICE Floating electrode-dielectric barrier device (FE-DBD) cold atmospheric plasma (CAP)
  • DRUG Canthardin Collodion

Trial Details

FieldValue
Enrollment Target 17 participants
Start Date 2021-12-02
Est. Completion 2022-12-31
Phase Phase 4

What the Registry Record Tells You About NCT05070754

The ClinicalTrials.gov registry entry for NCT05070754 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 17 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Medical University of South Carolina, which has 755 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 3 interventions - of which Cryotherapy is the first listed.

NCT05070754 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT05070754 about?

NCT05070754 is a clinical study titled "Cold Atmospheric Plasma Device for Pediatric Molluscum and Verruca". This study is going to test a cold atmospheric plasma device (CAP), in particular a floating electrode-dielectric barrier device (FE-DBD), to treat warts and molluscum. The treatment device in this study generates cold atmospheric plasma (gaseous ionized molecules) to rid the virus from the body. Ba...

What is the current status of trial NCT05070754?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 17 participants. The study started on 2021-12-02. Estimated completion is 2022-12-31.

What interventions are being tested in trial NCT05070754?

The interventions under investigation include: Cryotherapy (DEVICE), Floating electrode-dielectric barrier device (FE-DBD) cold atmospheric plasma (CAP) (DEVICE), Canthardin Collodion (DRUG).

Who is sponsoring clinical trial NCT05070754?

This trial is sponsored by Medical University of South Carolina, which has 755 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.