CellFX System for the Treatment of Cutaneous Non-Genital Warts

Pulse Biosciences

Status

Completed

Conditions

Warts Hand

Verruca

Warts

Treatments

Device: CellFX Device

Study type

Interventional

Funder types

Industry

Identifiers

NCT04554394

NP-WP-010

Details and patient eligibility

About

This prospective, non-randomized, multicenter pivotal study is designed to evaluate the safety and effectiveness of the CellFX System in patients with cutaneous non-genital warts on all areas of the body, excluding the face.

Full description

The study will enroll healthy adult subjects with a minimum of two cutaneous non-genital warts, excluding the face, with each wart lesion not exceeding 10 x 10mm. One of the warts for each subject will be untreated and will serve as the subject's internal control. Macrophotography of all study warts will be captured along with Investigator assessments using the Wart Measurement Scale (WMS) and lesion measurements for wart reduction. All subjects will be followed at 7, 30, 60, 90 and 120-days post-initial CellFX treatment. All wart lesions are eligible for re-treatment up to 3 times over the course of the study. Adverse events will be documented.

Enrollment

62 patients

Sex

All

Ages

21 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Subjects must be at least 21 and not older than 80 years of age
Subjects must be able to read and speak English or Spanish
Subjects must sign a written informed consent to participate in the study, prior to any study related procedures
Subject must have a minimum of two cutaneous non-genital warts, each not exceeding 10 x 10mm
Subject is willing to undergo all study-mandated procedures
Subject agrees to refrain from using all other wart removal products or treatments (topical medication including over-the-counter medications) during the study period

Exclusion criteria

Subject has an implantable electronic medical device. (pacemaker, implantable cardioverter defibrillator, etc.)
Subject has cochlear implants
Subject has an active systemic infection or history of an infection in the designated treatment area within 90 days of enrollment
Subject has a history of and/or current tinnitus
Subject is known to be immune-compromised
Subject is taking a blood thinning medication (Antiplatelet, Anticoagulation, Factor Xa Inhibitor, etc.)
Subject has Type 1 Diabetes and is insulin dependent
Subject has a known allergy to Lidocaine or Lidocaine-like products
Subject is a member of a vulnerable population including individuals employed by the Sponsor, clinic site, or entity associated with the conduct of the study
Subject has a comorbidity or condition which may reduce compliance with this protocol, including follow-up visits
Subject is participating in another research study involving an investigational agent (pharmaceutical, biologic, or medical device)