Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Comparing two types of dressings for preventing pressure ulcers in cardiac surgery patients

Official title: Effectiveness of Polyurethane Foam (Pink Pad) Compared With Mepilex Dressing for Pressure Ulcer Prevention in Operating Room: A Randomized Control Clinical Trial

Run by King Abdullah Medical City · NCT06790277 · Data updated 2026-11-12

This study is testing which type of dressing, either polyurethane foam or Mepilex, works better to prevent pressure ulcers in patients having heart surgery.

More Pressure Ulcer trials

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment100 (estimated)
SponsorKing Abdullah Medical City
Government
Locations1 site (Mecca, Western Reagan)
StatusRecruiting
StartedOctober 10, 2023
Main results expectedOctober 10, 2025
Study endsOctober 10, 2025
Registry record updatedJanuary 24, 2025
Trial IDNCT06790277 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are adults aged 18 and older who are undergoing cardiac surgery and are at risk for pressure ulcer development.

Probably not a fit

Patients under 17 years old or those with hypersensitivity to the dressing materials may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study aims to compare the effectiveness of polyurethane foam (Pink Pad) and Mepilex dressings in preventing pressure ulcers in patients undergoing cardiac surgery at King Abdullah Medical City. Both interventions will be applied in conjunction with standard care protocols, which include risk assessment using the Braden Scale. The study will evaluate the outcomes of each dressing type in terms of pressure ulcer prevention during surgical procedures. Participants will be monitored for their skin integrity and overall health status post-surgery.

Why it matters

Potential benefit: If successful, this study could lead to improved methods for preventing pressure ulcers in patients undergoing cardiac surgery.

How similar studies have gone: Previous studies have shown success in using similar dressing approaches for pressure ulcer prevention, indicating potential for positive outcomes in this study.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Subjects ≥ 18.
* Willing to participate.
* Patients undergoing cardiac surgery.
* Patient who is at risk for PU development as measured with Braden scale.
* Patient who has skin intact and having a life expectancy greater than 72 hours as per clinical judgement.

Exclusion Criteria:

* Subjects under 17
* Not consenting to participate
* Patients with suspected hypersensitivity reactions to any of the dressing formulation's ingredients.
* Patients who are unable to continue the study because of death or change in the care setting.

Where it's running

  • King Abdulla Medical City in Holy capital
    Mecca, Western Reagan, Saudi Arabia
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.