Chronic Postoperative Pain After Laparoendoscopic Groin Hernia Repair
CompletedNCT04838028
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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)
The study attempts to quantify the relative risks for chronic postoperative inguinal pain (CPIP) depending on different combinations of mesh and mesh fixation. For this purpose the investigators will analyze data from the Swedish Hernia Registry (SHR).
Study details
- Official title
- Mesh and Fixation Combinations in Laparoendoscopic Groin Hernia Repair: Association With Chronic Postoperative Pain. A Swedish Hernia Registry Study.
- Conditions
- Interventions
- Procedure: TEP
- Procedure: TAPP
- Procedure: Other or unspecified laparoendoscopic groin hernia repair
- Sponsor
- Karolinska Institutet
- Collaborators
- Uppsala University; Swedish Hernia Registry
- Start date
- 2012-09-01
- Primary completion
- 2019-12-31
- Sex
- All
- Age range
- from 15 Years
- Results posted
- No results posted in this snapshot
- Total sites listed
- 0
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: All laparoendoscopic repairs for groin hernia that have been registered in the SHR from September 1, 2012, until December 31, 2018. Exclusion Criteria: * Open repairs. * Hernioplasties that were converted from laparoscopic to open surgery. * Bilateral repairs. * Surgery merely for hernia (eg obturator) other than lateral, medial or femoral. * Age \< 15 years. * Patients not having a 10-digit state-assigned Patient Identification Number.
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT04838028