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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00405834
Other study ID # CR-0065
Secondary ID
Status Completed
Phase N/A
First received November 28, 2006
Last updated July 1, 2008
Start date June 2007
Est. completion date October 2007

Study information

Verified date June 2007
Source Hill-Rom
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

This study is to evaluate the clinical safety and effectiveness of the Envision® surface.


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 information / eligibility

Status Completed
Enrollment 30
Est. completion date October 2007
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility 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

Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Device:
Envision® Patient Support System


Locations

Country Name City State
United States Sinai Hospital of Baltimore Baltimore Maryland

Sponsors (1)

Lead Sponsor Collaborator
Hill-Rom

Country where clinical trial is conducted

United States, 

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