Skin Dressings Versus Lubrication to Prevent Pressure Ulcers: A Randomized Trial (PENFUP)
Primary Purpose
Pressure Ulcer
Status
Terminated
Phase
Phase 3
Locations
Colombia
Study Type
Interventional
Intervention
Skin dressing
Moisturizing cream
Sponsored by
About this trial
This is an interventional prevention trial for Pressure Ulcer focused on measuring Prevention, Pressure ulcers, Clinical trial, Nursing
Eligibility Criteria
Inpatients will be eligible if meeting two criteria:
- Intact skin on hospital admission
- High/very high risk of PU (Braden´s scale ≤ 20 points) will be eligible.
Exclusion Criteria:
- Treating physician disagree with participation
- Need for chronic use of diapers
Sites / Locations
- Fundación Cardioinfantil Instituto de Cardiología
- Clinica Carlos Ardila Lulle-FOSCAL
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Skin Dressing
Moisturizing cream
Arm Description
Hydrocolloid dressings applied during hospitalization
Use of moisturizing cream, as part of conventional skin care
Outcomes
Primary Outcome Measures
Pressure ulcers
First skin ulcer identified in the covered body areas
Secondary Outcome Measures
Length of stay
Total stay in hours
Time to the first walk
First walk out of bed as registered in patients' charts
Total cost of hospitalization
Total bill to insurer
Full Information
NCT ID
NCT02565745
First Posted
September 29, 2015
Last Updated
March 16, 2018
Sponsor
Fundación Cardioinfantil Instituto de Cardiología
1. Study Identification
Unique Protocol Identification Number
NCT02565745
Brief Title
Skin Dressings Versus Lubrication to Prevent Pressure Ulcers: A Randomized Trial
Acronym
PENFUP
Official Title
Impact of Skin Dressings Compared With Cream for Skin Lubrication in the Prevention of Pressure Ulcers in Patients at High or Very High Risk: A Multicenter Randomized Trial
Study Type
Interventional
2. Study Status
Record Verification Date
June 2017
Overall Recruitment Status
Terminated
Why Stopped
Recommendation after interim analysis
Study Start Date
December 2015 (undefined)
Primary Completion Date
August 31, 2017 (Actual)
Study Completion Date
December 12, 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Fundación Cardioinfantil Instituto de Cardiología
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Study purpose:
To assess if - in adult patients admitted to hospital with surgical or medical conditions at high/very high risk of developing pressure ulcers (PU) according to Braden scale - using skin dressing protection versus conventional care (lubricant or moisturizer cream) may prevent the incidence of in-hospital PU
Detailed Description
Participants will receive, in addition to the experimental/control interventions, background skin care measures, including anti- bedsore mattresses; body position changes every two hours, and shear/friction reduction.
Trained nurses will review all participants' charts and verify any report of PU until the first ambulation, discharge or death. Patients with a verified PU are referred to the institutional wound care group.
For the purpose of outcome adjudication, study personnel will email digital pictures to 2 independent, blinded outcome assessors (experts in skin care). Skin lesions will be rated in 4-level scale (EPUAP/NPUAP). In case of disagreement, a single, independent referee will confirm the presence/absence of any potential PU.
The unit for analysis will be patients developing (first occurrence, in a time-to-event analysis) PUs in the areas covered by the interventions.
See further details on eligibility, interventions and study outcomes below
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pressure Ulcer
Keywords
Prevention, Pressure ulcers, Clinical trial, Nursing
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Masking Description
Outcome assessors unaware of the treatment allocation will be sent photographs of the target skin areas with suspected PUs.
Allocation
Randomized
Enrollment
689 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Skin Dressing
Arm Type
Experimental
Arm Description
Hydrocolloid dressings applied during hospitalization
Arm Title
Moisturizing cream
Arm Type
Active Comparator
Arm Description
Use of moisturizing cream, as part of conventional skin care
Intervention Type
Combination Product
Intervention Name(s)
Skin dressing
Other Intervention Name(s)
Hydrocolloid dressing
Intervention Description
Pre-determined skin areas at risk for PUs (3 or more, depending on the prevaliing body position, prone, supine or Sims') will be covered. Dressings will be changed every 6-7 days unless found wet/contaminated
Intervention Type
Other
Intervention Name(s)
Moisturizing cream
Other Intervention Name(s)
Skin lubricant
Intervention Description
It will be applied twice a day to the same skin areas as the experimental group
Primary Outcome Measure Information:
Title
Pressure ulcers
Description
First skin ulcer identified in the covered body areas
Time Frame
During hospitalization
Secondary Outcome Measure Information:
Title
Length of stay
Description
Total stay in hours
Time Frame
During hospitalization
Title
Time to the first walk
Description
First walk out of bed as registered in patients' charts
Time Frame
During hospitalization
Title
Total cost of hospitalization
Description
Total bill to insurer
Time Frame
During hospitalization
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inpatients will be eligible if meeting two criteria:
Intact skin on hospital admission
High/very high risk of PU (Braden´s scale ≤ 20 points) will be eligible.
Exclusion Criteria:
Treating physician disagree with participation
Need for chronic use of diapers
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Olga L Cortés, RN,MSC,PhD
Organizational Affiliation
Fundacion Cardioinfantil Instituto de Cardiología
Official's Role
Principal Investigator
Facility Information:
Facility Name
Fundación Cardioinfantil Instituto de Cardiología
City
Bogotá
State/Province
Cundinamarca
Country
Colombia
Facility Name
Clinica Carlos Ardila Lulle-FOSCAL
City
Bucaramanga
State/Province
Santander
Country
Colombia
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
9766454
Citation
Bergstrom N, Braden B, Kemp M, Champagne M, Ruby E. Predicting pressure ulcer risk: a multisite study of the predictive validity of the Braden Scale. Nurs Res. 1998 Sep-Oct;47(5):261-9. doi: 10.1097/00006199-199809000-00005.
Results Reference
result
PubMed Identifier
23955535
Citation
Moore ZE, Webster J. Dressings and topical agents for preventing pressure ulcers. Cochrane Database Syst Rev. 2013 Aug 18;(8):CD009362. doi: 10.1002/14651858.CD009362.pub2.
Results Reference
result
Citation
McInnes E., Jammali-Blasi A., Bell-Syer S., Dumville JC., Cullum N. Support surfaces for pressure ulcer prevention (Review). The Cochrane Library. Published Online: 13 Apr 2011.http://www.thecochranelibrary.com.wiley.com/doi/10.1002.
Results Reference
result
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Skin Dressings Versus Lubrication to Prevent Pressure Ulcers: A Randomized Trial
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