A single-center, prospective, randomized, open-label, clinical trial of ceramide 2-containing hydrocolloid dressings versus polyurethane film dressings for pressure ulcer prevention in high-risk surgical patients
Not Applicable
- Conditions
- Pressure ulcer
- Registration Number
- JPRN-UMIN000019420
- Lead Sponsor
- Pressure Ulcer Committee of Tokyo Medical University Ibaraki Medical Canter
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 128
Inclusion Criteria
Not provided
Exclusion Criteria
Patient who did not written informed consent to participate. Patients with existing pressure damage and/or with a history of pressure ulcer at the intervention sites.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The incidence rate of pressure ulcer development in high-risk surgical patients in both groups.The development of a pressure ulcer was visually observed by one WOC nurse within 24 hours postsurgery.
- Secondary Outcome Measures
Name Time Method Incidence of skin damage, such as blanchable erythema, skin discoloration, contact dermatitis, and stripped skin, at the intervention sites.