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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00395980
Other study ID # 2006-5106
Secondary ID
Status Completed
Phase N/A
First received November 2, 2006
Last updated December 11, 2008
Start date October 2006
Est. completion date July 2007

Study information

Verified date December 2008
Source University of California, Irvine
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

Using healthy volunteers, participants will lay on an operating room table in various positions employed during kidney surgery. Using a pressure sensor mat, we hope to determine which areas of the body are subject to higher pressures. Using padding devices (foam, gel, water mattress)which are currently used in the operating room will be employed and measurements will be taken to determine which padding material and configurations is optimal to reduce the pressure to those body parts at risk for excessive pressure subject during laparoscopic surgery.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date July 2007
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Exclusion Criteria:

- Subjects with musculoskeletal disabilities

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Device:
surgical table pressure mat


Locations

Country Name City State
United States University of California, Irvine Medical Center Orange California

Sponsors (1)

Lead Sponsor Collaborator
University of California, Irvine

Country where clinical trial is conducted

United States, 

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