Envision® Surface Evaluation
Completed
- Conditions
- Pressure Ulcer
- Registration Number
- NCT00405795
- Lead Sponsor
- Hill-Rom
- Brief Summary
This observational study will acquire initial clinical practice utilization and product safety data for the Envision® surface.
- Detailed Description
This is a single site, open label, observational study to acquire initial clinical practice utilization information, product safety, and wound healing data, as defined by changes in wound volume and/or surface area, for patients with pressure ulcers placed on this surface.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
- Subject Weight < 400 lbs. Subject has Stage II, III, or IV pressure ulcer on weight bearing aspect of the body Subject estimated length of stay at least 7 days Subject Ability to provide informed consent
Exclusion Criteria
- Inability to provide informed 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)
Levindale Hebrew Geriatric Center and Hospital
🇺🇸Baltimore, Maryland, United States