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.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 100 (estimated) |
| Sponsor | King Abdullah Medical City Government |
| Locations | 1 site (Mecca, Western Reagan) |
| Status | Recruiting |
| Started | October 10, 2023 |
| Main results expected | October 10, 2025 |
| Study ends | October 10, 2025 |
| Registry record updated | January 24, 2025 |
| Trial ID | NCT06790277 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
- Study coordinator: Wedian O. Almowallad / Head of Clinical Trial Department, Master
- Email: Almwlld.W@kamc.med.sa
- Phone: 012 5549999
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Multicenter test of several CAMP products plus standard care for nonhealing pressure ulcers
This trial tests five different CAMP products added to standard care to see if they help heal nonhealing pressure ulcers in adults.
-
THERAVEX Tissue Care Spray Plus for Healing of Skin Wounds and Ulcers
This observational review tests whether THERAVEX Tissue Care Spray Plus, used with standard wound care, helps heal various skin wounds and chronic ulcers in adults.
-
Using a handheld algometer to predict opioid needs during open-heart surgery
This will try to see if a preoperative pain threshold measured with a handheld algometer can predict how much opioid pain medicine patients need during and after elective cardiac surgery.
-
Single-layer amniotic membrane (XPURT) plus standard care for chronic pressure ulcers
This project will try adding a single-layer amniotic membrane (XPURT) to standard wound care to see if it helps close nonhealing stage 3–4 pressure ulcers in adults.
-
Preventing pressure ulcers with gentle application of Rivadouce vegetable skincare oil
This project will test whether gently massaging Rivadouce vegetable skincare oil onto pressure-prone skin helps prevent pressure ulcers in adults at risk.
-
Cellular, acellular, and matrix wound products plus standard care for nonhealing stage 3–4 pressure ulcers
This study will try several cellular, acellular, and matrix-like wound products with standard care to see if adults with nonhealing stage 3–4 pressure ulcers heal more completely over 20 weeks than with standard care alone.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.