Actively Recruiting
Evaluation of a Switchable Acrylic Adhesive Drape for Safer Removal in Negative Pressure Wound Therapy Applications.
Led by Global Biomedical Technologies, LLC · Updated on 2026-04-24
300
Participants Needed
6
Research Sites
83 weeks
Total Duration
On this page
Sponsors
G
Global Biomedical Technologies, LLC
Lead Sponsor
N
National Institute for Biomedical Imaging and Bioengineering (NIBIB)
Collaborating Sponsor
AI-Summary
What this Trial Is About
Negative pressure wound therapy (NPWT) is widely used for chronic and acute wounds, severe burns, and post-operative care. Despite its benefits, the strong adhesive required to maintain an airtight seal increases the risk of medical adhesive-related skin injuries (MARSI), pain, and discomfort during removal. Global Biomedical Technologies (GBT) aims to develop an NPWT drape with "switchable adhesive" technology to enhance removal while maintaining an effective seal. This innovation is expected to benefit both single-use and serial-use NPWT applications by reducing MARSI and improving patient comfort. This project will compare the functionality and acceptability of Comfort Release® NPWT drapes with the industry-standard V.A.C. drape (KCI Technologies, Inc.), or other facility standard drape, in a non-blinded randomized controlled trial. Specific Aims Aim 1: Compare Comfort Release® drapes with V.A.C. drapes in single-use NPWT applications in post-surgical patients (n=200) at Columbia University Medical Center, Weill Cornell Medical Center, and Absolute Medical Center. Milestones: Demonstrate statistically significant (α=0.05) improvement over V.A.C. drapes in: Reduction of MARSI (Medical Adhesive-Related Skin Injury scoring system) Decreased pain (Indiana Polyclinic Combined Pain Scale) Reduced need for pain/anxiety medication Equivalent or improved seal effectiveness (leak incidence rate) Clinician acceptability Reduced nursing time by ≥20% Economic value through time and cost savings Aim 2: Compare Comfort Release® drapes with V.A.C. drapes in serial-use NPWT applications in chronic wound patients (n=100) at Weill Cornell Medical Center, Vital Medical Research, and All South Bay Footcare. Patients will undergo approximately three NPWT drape changes per week. Milestones: Demonstrate statistically significant (α=0.05) improvement over V.A.C./or standard drapes in: Reduction of MARSI Decreased pain (Indiana Polyclinic Combined Pain Scale) Improved compliance with treatment duration Reduced need for pain/anxiety medication Equivalent or better seal effectiveness Clinician acceptability (questionnaire score \>4) Reduced nursing time by ≥20% Economic value through time and cost savings At each dressing change and at final removal, qualitative data from clinicians will be collected to assess the acceptability and usability of Comfort Release® NPWT drapes.
CONDITIONS
Official Title
Evaluation of a Switchable Acrylic Adhesive Drape for Safer Removal in Negative Pressure Wound Therapy Applications.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 18 years or older post-surgical inpatients with a plan of treatment using NPWT
- Able to communicate and consent to participation in the study
- Access to V.A.C. by KCI drape and NPWT kits
- Able to report pain level using a pain scale
- If outpatient, able to return to the clinic for all drape/dressing changes
You will not qualify if you...
- History of known hypersensitivity to acrylic adhesives
- History of known hypersensitivity to isopropyl alcohol
- Patient expected to be unconscious during the drape removal/change
- Under the age of 18 years
- Unable to give consent, including due to language barrier unless an interpreter is readily available
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 6 locations
1
Eazy Foot & Ankle
Los Angeles, California, United States, 90035
Not Yet Recruiting
2
All South Bay Footcare/Podiatry Group, Inc.
Torrance, California, United States, 90505
Not Yet Recruiting
3
Absolute Medical Center, LLC
Miami, Florida, United States, 33126
Actively Recruiting
4
Vital Medical Research
Sweetwater, Florida, United States, 33174
Actively Recruiting
5
Columbia University Medical Center
New York, New York, United States, 10032
Active, Not Recruiting
6
Weill Cornell Medical Center
New York, New York, United States, 10065
Actively Recruiting
Research Team
H
Howard S Rosing, Sponsor, MD, PhD
CONTACT
D
Denise L Anderson, Director of Clinical Operations & Communications, RN, WCC
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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