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Clinical trialNCT00771407CompletedPhase 4Interventional

Parastomal Reinforcement With Strattice

SponsorLifeCellEnrollment120Parastomal Hernia
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

The purpose of this study is to compare the clinical outcomes of patients undergoing surgery for a permanent abdominal wall ostomy with and without placement of Strattice fascial inlay, as measured by postoperative occurence of parastomal hernia.

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

23 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • University of South Alabama

    Mobile, Alabama, United States

  • Office of Dr Phillip Fleshner

    Los Angeles, California, United States

  • University of California at Irvine

    Orange, California, United States

  • Stanford University Medical Center

    Stanford, California, United States

  • University of South Florida

    Tampa, Florida, United States

  • Cleveland Clinic Florida

    Weston, Florida, United States

  • University of Illinois

    Chicago, Illinois, United States

  • Indiana University Medical Center

    Indianapolis, Indiana, United States

  • Louisiana State University

    New Orleans, Louisiana, United States

  • Ochsner Clinic

    New Orleans, Louisiana, United States

  • University of Maryland/baltimore Va

    Baltimore, Maryland, United States

  • Spectrum Health - Butterworth Hospital

    Grand Rapids, Michigan, United States

  • Colon and Rectal Surgery Associates Ltd

    Saint Paul, Minnesota, United States

  • Washington University School of Medicine - Barnes Jewish West

    St Louis, Missouri, United States

  • Colon & Rectal Surgery Inc

    Omaha, Nebraska, United States

  • Albany Medical College

    Albany, New York, United States

  • Mt Sinai Medical Center

    New York, New York, United States

  • Stony Brook University Medical Center

    Stony Brook, New York, United States

  • Duke University Medical Center

    Durham, North Carolina, United States

  • the Christ Hospital Research

    Cincinnati, Ohio, United States

  • Cleveland Clinic

    Cleveland, Ohio, United States

  • the Methodist Hospital

    Houston, Texas, United States

  • University of Vermont

    Burlington, Vermont, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study. It may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
31 Dec 2008
Primary completion
29 Feb 2012
Completion
31 Jul 2012
Last update posted
28 Sept 2015
Registered enrollment
120
Registry id
NCT00771407

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.