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Flemish Inguinal and Femoral Hernia Prospective Registry

NCT04623580 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 560

Last updated 2024-07-01

No results posted yet for this study

Summary

Prospective registry. The purpose of this clinical trial will be to measure surgical outcome parameters (e.g. recurrence, chronic pain and other quality indicators) after inguinal hernia repair using Patient Reported Outcome Measures (PROMs) in the short- and long-term.

Conditions

  • Inguinal Hernia

Interventions

DEVICE

Surgical inguinal or femoral hernia repair

Surgical inguinal or femoral hernia repair (primary or mesh)

Sponsors & Collaborators

  • Universitaire Ziekenhuizen KU Leuven

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-01-01
Primary Completion
2028-12-31
Completion
2028-12-31
FDA Device
Yes

Countries

  • Belgium

Study Locations

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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 NCT04623580 on ClinicalTrials.gov