Bassini Inguinal Hernia Repair: Obsolete Or Still A Viable Surgical Option?

May 11, 2021 updated by: Jeannie Rivers, Hunter Holmes Mcguire Veteran Affairs Medical Center

Incidence of POUR in the Veteran Population After Elective Inguinal Hernia Repair: A Retrospective Study

Retrospective review of hernia surgery patients at HHMcGuire VAMC focusing on repair type and postoperative complications.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Observational

Enrollment (Actual)

203

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • United States
    • Virginia
      • Richmond, Virginia, United States, 23249
        • Hunter Holmes McGuire VAMC

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Veterans who underwent inguinal hernia repair without mesh

Description

Inclusion Criteria: Inguinal hernia repair without mesh -

Exclusion Criteria: Mesh repair

-

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Inguinal hernia recurrence
Time Frame: 5-13 years postoperatively
chart review
5-13 years postoperatively

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
wound infection
Time Frame: 5-13 years
chart review
5-13 years
urinary retention
Time Frame: 5-13 years
chart review
5-13 years
groin pain
Time Frame: 5-13 years
chart review
5-13 years
durability of repair
Time Frame: 5-13 years postop
chart review
5-13 years postop
testicular ischemia
Time Frame: 5-13 years
chart review
5-13 years

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Hunter Holmes Mcguire Veteran Affairs Medical Center

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

January 1, 2006

Primary Completion (ACTUAL)

December 31, 2014

Study Completion (ACTUAL)

December 31, 2019

Study Registration Dates

First Submitted

May 11, 2021

First Submitted That Met QC Criteria

May 11, 2021

First Posted (ACTUAL)

May 17, 2021

Study Record Updates

Last Update Posted (ACTUAL)

May 17, 2021

Last Update Submitted That Met QC Criteria

May 11, 2021

Last Verified

May 1, 2021

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 02331

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

All personally identifiable information is secured. Study outcomes reported in aggregate only.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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