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NCT02759900 Clinical Trial

Using a Cold Atmospheric Plasma Device to Treat Skin Disorders

Actinic Keratosis Clinical Trial

Official title:
Using a Cold Atmospheric Plasma Device to Treat Skin Disorders

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT02759900
Other study ID # 20130084
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date January 2016
Est. completion date January 2025

Study information
Verified date April 2022
Source The Skin Center Dermatology Group
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study examines the efficacy of a non-thermal, atmospheric plasma device in the treatment of skin disorders

Description:

The study uses non-thermal atmospheric pressure plasma to treat target conditions. The patients are monitored at set intervals for efficacy and adverse effects using investigator's assessment and imaging techniques

Recruitment information / eligibility
Status Recruiting
Enrollment 100
Est. completion date January 2025
Est. primary completion date March 2024
Accepts healthy volunteers No
Gender All
Age group 4 Years and older
Eligibility Inclusion Criteria: - diagnoses of target conditions - ability to complete study protocol Exclusion Criteria: - based on specific condition

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• Non-thermal, atmospheric plasma to treat skin lesions and acne
Non-thermal, atmospheric plasma treatment of affected area or lesions using a nanosecond dielectric barrier discharge plasma device
• Indirect non-thermal, atmospheric plasma to treat hair loss and acne
A compound of non-thermal, atmospheric plasma and medium is delivered to or generated at the target area. Plasma is generated using either microsecond dielectric barrier discharge plasma device or PiezoBrush (a helium jet plasma). The medium is an aqueous alcohol solution

Locations
Country Name City State
United States The Skin Center Dermatology Group New City New York

Sponsors (1)
Lead Sponsor Collaborator
The Skin Center Dermatology Group

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Clinical improvement The outcome is the presence or lack of clinical improvement in the investigator's global assessment and reviewing photo-documentation as well as reflectance confocal microscopy study investigator's global assessment and reviewing photo-documentation 1-12 months
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