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Chronic Postoperative Pain After Laparoendoscopic Groin Hernia Repair

NCT04838028 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 15360

Last updated 2025-07-01

No results posted yet for this study

Summary

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).

Conditions

Interventions

PROCEDURE

TEP

Laparoendoscopic totally extraperitoneal mesh repair of groin hernia

PROCEDURE

TAPP

Laparoscopic transabdominal mesh repair of groin hernia

PROCEDURE

Other or unspecified laparoendoscopic groin hernia repair

"Other" refers to any laparoendoscopic mesh repair specified as not being either TEP or TAPP, eg, "intraperitoneal onlay mesh" (IPOM).

Sponsors & Collaborators

  • Uppsala University

    collaborator OTHER

  • Swedish Hernia Registry

    collaborator UNKNOWN

  • Karolinska Institutet

    lead OTHER

Principal Investigators

  • Bengt Novik, MD · Dept of Clinical Sciences, Karolinska Institutet, Danderyd Hospital, Stockholm

Eligibility

Min Age
15 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-09-01
Primary Completion
2019-12-31
Completion
2020-11-06

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04838028 on ClinicalTrials.gov