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Muscle Pressure in the Flank Position

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00395980
First Posted: November 6, 2006
Last Update Posted: December 12, 2008
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
University of California, Irvine
  Purpose
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.

Condition Intervention
Tissue Breakdown Device: surgical table pressure mat

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Prevention
Official Title: Muscle Pressure in the Flank Position

Further study details as provided by University of California, Irvine:

Enrollment: 20
Study Start Date: October 2006
Study Completion Date: July 2007
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Exclusion Criteria:

  • Subjects with musculoskeletal disabilities
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00395980


Locations
United States, California
University of California, Irvine Medical Center
Orange, California, United States, 92868
Sponsors and Collaborators
University of California, Irvine
Investigators
Principal Investigator: Leslie A. Deane, MD University of California, Irvine
  More Information

Responsible Party: Leslie Deane, MD, University of California, Irvine
ClinicalTrials.gov Identifier: NCT00395980     History of Changes
Other Study ID Numbers: 2006-5106
First Submitted: November 2, 2006
First Posted: November 6, 2006
Last Update Posted: December 12, 2008
Last Verified: December 2008