Envision® Surface Evaluation

Hill-Rom

Status: Completed

Conditions: Pressure Ulcer

Treatments: Device: Envision® Patient Support System

Study type: Observational

Funder types: Industry

Identifiers

NCT00405795

MR-2005-083

Details and patient eligibility

About

This observational study will acquire initial clinical practice utilization and product safety data for the Envision® surface.

Full 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.

Enrollment: 30 patients

Sex: All

Volunteers: No Healthy Volunteers

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