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Completed Phase 3 Interventional

Does Tension-Free Herniorrhaphy or Laparoscopic Herniorrhaphy Achieve Equal or Better Recurrence Rates and Lower Costs While Achieving Equivalent Outcomes for Hernia Patients?

ClinicalTrials.gov ID: NCT00032448

Public ClinicalTrials.gov record NCT00032448. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 6, 2026, 4:33 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

CSP #456 - Tension Free Inguinal Hernia Repair: Comparison of Open and Laparoscopic Surgical Techniques

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Inguinal hernia is one of the most common worldwide afflictions of men. The presence of an inguinal hernia is indication for its repair. Approximately 700,000 hernia repairs are performed in the U.S. each year, and this procedure accounts for 10% of all general surgery procedures in the Veterans Health Administration (VHA) (10,000 inguinal herniorrhaphies performed per year). There are many different techniques currently in use for repairing inguinal hernias and with the advent of laparoscopy, yet another technique is being advocated. Laparoscopic repair has been reported in some studies to be superior to open repair because of less pain and earlier return to work. However, laparoscopic repair requires a general or regional anesthetic and expensive equipment and supplies to perform. There is also evidence that open tension-free mesh repair may have results similar to laparoscopic repair for these patient centered outcome measures. The general acceptance of this procedure, especially in the VHA, has not been uniform. Furthermore, no randomized trial of sufficient size and power to be conclusive has been done to set forth the operative "gold standard" for hernia repair.

Study identification

NCT ID
NCT00032448
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Enrollment
2,200 participants

Conditions and interventions

Conditions

Eligibility (public fields only)

Age range
18 Years and older
Sex
Male
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 30, 1998
Primary completion
Nov 30, 2003
Completion
May 31, 2004
Last update posted
Apr 13, 2011

1998 – 2004

United States locations

U.S. sites
14
U.S. states
12
U.S. cities
14
Facility City State ZIP Site status
VA Medical Center, Birmingham Birmingham Alabama 35233
Central Arkansas VHS Eugene J. Towbin Healthcare Ctr, Little Rock No. Little Rock Arkansas 72114-1706
VA Medical Center, San Francisco San Francisco California 94121
VA Greater Los Angeles Healthcare System, West LA West Los Angeles California 90073
James A. Haley Veterans Hospital, Tampa Tampa Florida 33612
VA Maryland Health Care System, Baltimore Baltimore Maryland 21201
VA Medical Center, Jamaica Plain Campus Boston Massachusetts 02130
John D. Dingell VA Medical Center, Detroit Detroit Michigan 48201
VA Medical Center, Durham Durham North Carolina 27705
WJB Dorn Veterans Hospital, Columbia Columbia South Carolina 29209
VA Medical Center, Memphis Memphis Tennessee 38104
VA North Texas Health Care System, Dallas Dallas Texas 75216
Michael E. DeBakey VA Medical Center (152) Houston Texas 77030
VA Salt Lake City Health Care System, Salt Lake City Salt Lake City Utah 84148

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00032448, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 13, 2011 · Synced Sep 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00032448 live on ClinicalTrials.gov.

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