New York, NYNCT06717308Now EnrollingIRB Ready

Frequency and Type of Medical Adhesive-Related Skin Injury Clinical Trial in New York, NY

Access cutting-edge frequency and type of medical adhesive-related skin injury treatment through this clinical trial at a research site in New York. Study-provided care at no cost to qualified participants.

Sponsored by Global Biomedical Technologies, LLC

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Expert Care in New York

Access frequency and type of medical adhesive-related skin injury specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related frequency and type of medical adhesive-related skin injury treatment provided free

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Check if you qualify for this frequency and type of medical adhesive-related skin injury clinical trial in New York, NY

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Why Participate?

  • No-Cost Study Care

  • Local to New York

    Convenient for NY residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit New York site if eligible
  4. 4Begin participation

About This Frequency and Type of Medical Adhesive-Related Skin Injury Study in New York

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 ReleaseĀ® 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 ReleaseĀ® 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 ReleaseĀ® 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 ReleaseĀ® NPWT drapes.

Sponsor: Global Biomedical Technologies, LLC

Who Can Participate

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.

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in New York?

Yes, this clinical trial (NCT06717308) has an active research site in New York, NY that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Frequency and Type of Medical Adhesive-Related Skin Injury Treatment Options in New York, NY

If you're searching for frequency and type of medical adhesive-related skin injury treatment options in New York, NY, this clinical trial (NCT06717308) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our New York research site is actively enrolling participants for this clinical trial. You'll receive care from experienced frequency and type of medical adhesive-related skin injury specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all frequency and type of medical adhesive-related skin injury clinical trials near you to find additional studies recruiting in your area.

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