Envision® Surface Evaluation

Envision® Surface Evaluation for Patients With Stage II, Stage III, or Stage IV Pressure Ulcers

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT00405795

Enrollment

Registered

2006-11-30

Start date

2007-06-30

Completion date

2008-03-31

Last updated

2008-07-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pressure Ulcer

Keywords

Pressure Ulcer

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.

Interventions

DEVICEEnvision® Patient Support System

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

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

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026