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Terminated Not applicable Interventional Results available

Clinical Study to Assess a New Barrier Film's Ability to Provide Skin Protection Against Incontinence & Allow Healing

ClinicalTrials.gov ID: NCT02570139

Public ClinicalTrials.gov record NCT02570139. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 23, 2026, 1:28 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Multi-Center, Randomized Trial Comparing the Efficacy of 3M™ Cavilon™ Advanced Barrier Film for the Treatment of Incontinence-associated Dermatitis to a Commercially Available Moisture Barrier

Study identification

NCT ID
NCT02570139
Recruitment status
Terminated
Study type
Interventional
Phase
Not applicable
Lead sponsor
Solventum US LLC
Industry
Enrollment
45 participants

Conditions and interventions

Interventions

  • Cavilon Advanced Skin Protectant Device
  • ConvaTec Sensi-Care Protective Barrier Device

Device

Eligibility (public fields only)

Age range
1 Hour and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 30, 2015
Primary completion
Jun 22, 2017
Completion
Jun 22, 2017
Last update posted
Oct 1, 2024

2015 – 2017

United States locations

U.S. sites
10
U.S. states
7
U.S. cities
10
Facility City State ZIP Site status
Children's Hospitals and Clinic Minneapolis Minnesota 55404
Children's Hospital and Clinics Saint Paul Minnesota 55102
Good Samaritan Kearney Nebraska 68848
St. Elizabeth Lincoln Nebraska 68510
Hackensack University Medical Center Hackensack New Jersey 76010
North Shore University Hospital Manhasset New York 11030
Lennox Hill New York New York 10075
St. John Tulsa Oklahoma 74104
Roper St. Francis Charleston South Carolina 29401
Baylor Plano Plano Texas 75093

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02570139, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 1, 2024 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02570139 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →