Envision® Surface Evaluation

Hill-Rom30 enrolled

Overview

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

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.

Study Type

OBSERVATIONAL

Enrollment

Conditions

Pressure Ulcer

Interventions

Envision® Patient Support SystemDEVICE

Eligibility

Sex: ALL

Medical Language ↔ Plain English

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

Locations (1)

Levindale Hebrew Geriatric Center and Hospital

Baltimore, Maryland, United States

Data from ClinicalTrials.gov

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