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Chronic Postoperative Pain After the Lichtenstein Groin Hernioplasty

NCT04839848 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 80733

Last updated 2022-12-05

No results posted yet for this study

Summary

The study attempts to quantify the relative risks for chronic postoperative inguinal pain (CPIP) after Lichtenstein repair of groin hernia, depending on mesh type and fixation suture material.

For this purpose the investigators will analyze data from the Swedish Hernia Registry (SHR).

Conditions

  • Hernia, Inguinal
  • Hernia, Femoral
  • Postoperative Pain
  • Chronic Pain
  • PROM
  • Suture Related Complication

Interventions

DEVICE

Lichtenstein mesh repair

A groin hernia repair, reinforced by synthetic mesh. The mesh is affixed with sutures

Sponsors & Collaborators

  • Uppsala University

    collaborator OTHER

  • Swedish Hernia Registry

    collaborator UNKNOWN

  • Karolinska Institutet

    lead OTHER

Eligibility

Min Age
15 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-09-01
Primary Completion
2019-11-06
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 NCT04839848 on ClinicalTrials.gov