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Trunk Strength Study

This study has been completed.
Sponsor:
Information provided by:
University of Kentucky
ClinicalTrials.gov Identifier:
NCT01300936
First received: February 18, 2011
Last updated: March 10, 2011
Last verified: March 2011
  Purpose

The purpose of this study is to measure abdominal wall strength both preoperatively and postoperatively in patients undergoing ventral/incisional hernia repairs. The investigators hypothesize that abdominal wall strength is improved in hernia repairs that reapproximate the rectus musculature to the midline. Abdominal wall strength measurements would be obtained utilizing various abdominal strength testing.


Condition
Ventral/Incisional Hernia Repairs

Study Type: Observational
Study Design: Observational Model: Case Control
Time Perspective: Prospective
Official Title: Abdominal Wall Hernias and Abdominal Wall Function: A Quantitative Study of Trunk Strength.

Resource links provided by NLM:


Further study details as provided by University of Kentucky:

Estimated Enrollment: 10
Study Start Date: March 2010
Groups/Cohorts
patients with abdominal wall hernias

  Eligibility

Ages Eligible for Study:   18 Years to 65 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

Patients who will undergo laparoscopic ventral hernia repair or open repair. People between the ages of 18 to 65 in relative good health.

Criteria

Inclusion Criteria:

  • Patients who are scheduled for hernia repair.

Exclusion Criteria:

  • Pregnant females.
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01300936

Locations
United States, Kentucky
University of Kentucky Medical Center
Lexington, Kentucky, United States, 40536
Sponsors and Collaborators
University of Kentucky
Investigators
Principal Investigator: Scott Roth, MD University of Kentucky
  More Information

No publications provided

Responsible Party: John Scott Roth, MD, University of Kentucky Medical Center
ClinicalTrials.gov Identifier: NCT01300936     History of Changes
Other Study ID Numbers: 09-0876-P6H
Study First Received: February 18, 2011
Last Updated: March 10, 2011
Health Authority: United States: Institutional Review Board

Additional relevant MeSH terms:
Hernia
Pathological Conditions, Anatomical

ClinicalTrials.gov processed this record on November 25, 2014