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Trigger-point Blockade in Persistent Pain After Open Groin Hernia Repair

CompletedPhase 3NCT02065219
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)

Groin hernia repair is a common procedure performed in approximately 2,000 patients per one million inhabitants. Severe chronic pain following groin hernia repair is seen in 2-5% of the patients indicating that a large number of patients each year suffer from debilitating reduction in health-related quality of life. This study examines the effect of ultra-sound guided blocks with local anesthesia in the groin in regard to pain relief and sleep quality. The hypothesis of the study is that a block will confer significant pain relief to patients with severe chronic pain following open groin hernia repair.

Study details

Official title
Trigger-point Blockade in Persistent Pain After Open Groin Hernia Repair
Sponsor
University of Copenhagen
Collaborators
Copenhagen University Hospital, Rigshospitalet
Start date
2013-11
Primary completion
2014-04
Sex
All
Age range
from 18 Years
Healthy volunteers
true
Results posted
No results posted in this snapshot
Countries
Denmark
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Patients with persistent pain (\< 6 mo) after open groin hernia repair * Patients with maximal pain area 3 cm or less from the superficial inguinal ring * Patients living in the Capital Region of Denmark (Region Hovedstaden) or the Region of Zealand (Region Sjælland) Exclusion Criteria: * Known allergy to bupivacaine or other local anesthetics of amide-type * Declared incapable of making his/hers own affairs * Does not comprehend Danish in the written or spoken language * Cognitive impairment to a degree influencing the testing reliability * Known recurrence of the inguinal hernia * Other surgical procedures performed in the groin or on the external genitals * Neuropathy affecting the groin region caused by other conditions, e.g. post-stroke, multiple sclerosis, herniated intervertebral disc * Abuse of alcohol or drugs * Unable to cooperate with the sensory examinations

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT02065219