A Pilot Study of the Envision® Surface
Completed
- Conditions
- Pressure Ulcers
- Registration Number
- NCT00405834
- Lead Sponsor
- Hill-Rom
- Brief Summary
This study is to evaluate the clinical safety and effectiveness of the Envision® surface.
- Detailed Description
This study is to evaluate the clinical safety and effectiveness of the Envision® surface placed on the TotalCare® frame in pressure ulcer prevention and management, patient comfort, and staff acceptance in the critical care environment
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
- Subject weighs between 70 and 400 pounds Subject to remain on Envision Surface for at least 3 days Subject at risk for pressure ulcers (Braden Score < 14) or has existing ulcer of any stage Subject is able to provide voluntary consent
Exclusion Criteria
- Subject requires pulmonary treatment surface Subject declines consent
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Sinai Hospital of Baltimore
🇺🇸Baltimore, Maryland, United States