Evaluation of a Switchable Acrylic Adhesive Drape for Safer Removal in Negative Pressure Wound Therapy Applications.
Global Biomedical Technologies, LLC · with National Institute for Biomedical Imaging and Bioengineering (NIBIB), Weill Medical College of Cornell University · NCT06717308
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18+ · All sexes
- Healthy volunteers
- Not accepted (a condition is required)
- Study type
- Interventional · Not applicable
- Target enrollment
- 300
- US sites recruiting
- 3
- Study start
- February 10, 2025
- Record last updated
- October 21, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study 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 or short-term 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.
Being studied: Comfort Release® NPWT drape
Conditions: Frequency and Type of Medical Adhesive-Related Skin Injury; NPWT Drape Seal Effectiveness Rate (or Leak Incidence Rate); Clinician Acceptability of New NPWT Drape; Patient Drop-out Rate From Prescribed NPWT Treatment; Pain Assessment During Medical Adhesive Drape Removal
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- 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
Exclusion Criteria
- History of known hypersensitivity to acrylic adhesives
- History of known hypersensitivity to isopropyl alcohol
- The patient is expected to be unconscious during the drape removal/change
-NOTE: For the Weill Cornell Medicine site only: Patient is expected to be unconscious during ALL drape removal/changes.
- Under the age of 18 years 5. Unable to give consent, including a language barrier, unless an interpreter is readily available.
Recruiting US locations
Eazy Foot & Ankle
Los Angeles, CA 90035
Site contact: Rosie Berrios, Office Manager · 310-326-0202 · allsouthbayfootcare@gmail.com
All South Bay Footcare/Podiatry Group, Inc.
Torrance, CA 90505
Site contact: Rosie Berrios, Office Manager · 310-326-0202 · allsouthbayfootcare@gmail.com
Weill Cornell Medical Center
New York, NY 10065
Site contact: Amy Chun · chh4020@med.cornell.edu
Study contacts (from the official record)
- Howard S Rosing, Sponsor, MD, PhD · 239-330-5646 · hrosing@comfortrelease.com
- Denise L Anderson, Director of Clinical Operations & Communications, RN, WCC · 833-726-9269 · danderson@comfortrelease.com