Skip to content

Predisposing Factors for Chronic Postherniotomy Pain

CompletedNot applicableNCT00649142
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)

Chronic pain affects pain in 5-8% of patients more than a year after groin hernia repair. However no prospective study has investigated potential predisposing factors for development of pain, including genetic, psychosocial and detailed neurophysiological assessment of surgical method. The current study will assess the above factors in a prospective study.

Study details

Official title
Prospective Study of Predisposing Factors for Chronic Postherniotomy Pain
Conditions
  • Chronic Postherniotomy Pain
Interventions
  • Procedure: Open sutured mesh repair
  • Procedure: Laparoscopic mesh glue fixation
Sponsor
Copenhagen University Hospital, Rigshospitalet
Collaborators
Aesculap AG; Baxter Healthcare Corporation
Start date
2007-01
Primary completion
2008-09
Sex
Male
Age range
from 18 Years to 80 Years
Results posted
No results posted in this snapshot
Countries
Denmark, Germany
Total sites listed
2

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Adult (\>18 years) * Male * Primary unilateral groin hernia * Ability to use pain scales Exclusion Criteria: * Neurological disease * Diabetes with late stage complications

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT00649142