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Preoperative Etanercept Before Inguinal Hernia Surgery

CompletedNot applicableNCT00825344
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

Inguinal hernia repair is one of the most frequently performed operations in young men. Persistent pain after inguinal surgery represents a significant cause of disability, occurring in between 15%-35% of cases. In a majority of these patients, their groin pain persisted after a previous hernia repair. The main type of chronic postsurgical pain is neuropathic, caused by injured nerves. One of the principal components in the pathophysiology of postsurgical pain is cytokines, specifically tumor necrosis factor (TNF). In animal studies, injecting TNF inhibitors before nerve injury can reduce pain behaviors and neuropathology. Finding a way to reduce the incidence of postsurgical pain after hernia repair could enhance function, and reduce the need for opioids and other analgesics. The investigators intend to conduct the first randomized, controlled study evaluating whether preemptive administration of a tumor necrosis inhibitor can reduce postoperative pain and opioid consumption after hernia repair. This is important because the degree and intensity of postsurgical pain is a major predictor for the development of chronic postsurgical pain.

Study details

Official title
A Randomized Controlled Study Evaluating Pre-operative Etanercept on the Severity of Postoperative Pain After Inguinal Hernia Surgery.
Interventions
Sponsor
Johns Hopkins University
Collaborators
Walter Reed Army Medical Center; John P. Murtha Neuroscience and Pain Institute
Start date
2009-01
Primary completion
2011-11
Sex
All
Age range
from 18 Years to 70 Years
Results posted
Yes, on ClinicalTrials.gov
Countries
United States
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: 1. Demonstrable hernia evident using ultrasound, computed tomography, or on physical exam. 2. Pt scheduled for unilateral inguinal hernia repair. 3. Symptoms present for \< 6 months. Exclusion Criteria: 1. Non-elective surgery. 2. Previous hernia repair at the same site, or surgery near the site of the hernia. 3. Demyelinating neurological disease. 4. Current or recent (\< 6 years) history of substance abuse. 5. Pregnancy, which will be ruled out by a urine pregnancy test in women of childbearing age. 6. Pre-existing untreated psychiatric condition that could preclude an optimal treatment response (e.g. untreated posttraumatic stress disorder). 7. Unstable medical condition (e.g. unstable angina or congestive heart failure or severe). 8. Rheumatoid arthritis, or other systemic conditions that might respond to TNF inhibitors. 9. Pt is immunosuppressed or is taking other drugs (e.g. corticosteroids) that might suppress the immune system. 10. Systemic infection. 11. Any opioid analgesics within 48 hours of skin incision. 12. Any use of tricyclic antidepressants, serotoninin-norepinephrine reuptake inhibitors, or anticonvulsants within 72 hours of skin incision.

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT00825344