Autopsy report · NCT05937672

Cold Atmospheric Plasma Device Extension Study

Cause of deathOther Automatic label, confidence 0.3, unverified. How labels are made.

“Device needed repairs and delay this would cause would have affected data integrity if study were continued due to treatment delay.”

The sponsor’s own words in the registry.

Life of this trial

Registered 3 months before it started.
Ran for about 2 years 3 months before it stopped.
60 participants enrolled.
No results are posted on the registry.

Vital statistics

Status: Terminated
Phase: Phase 3
Sponsor: Medical University of South Carolina
Sponsor type: University, hospital or other
Conditions: Verruca Vulgaris; Molluscum Contagiosum
Interventions: Floating electrode-dielectric barrier device (FE-DBD) cold atmospheric plasma (CAP)
Participants: 60
Sites: 1
Countries: United States

Look deeper

The official registry record (the source of truth)
Record history: every change the sponsor made
Open it in the database

Everything here comes from the current ClinicalTrials.gov record. The timeline uses the record’s dates; dates marked planned are the sponsor’s plans. The cause of death is an automatic, unverified label. This is research information, not medical advice.