RecruitingNCT04623580
Flemish Inguinal and Femoral Hernia Prospective Registry
Sponsor
Universitaire Ziekenhuizen KU Leuven
Enrollment
560 participants
Start Date
Jan 1, 2018
Study Type
OBSERVATIONAL
Conditions
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.
Eligibility
Min Age: 18 Years
Inclusion Criteria8
- Consecutively all patients with a groin hernia (inguinal and/or femoral hernia) operated starting 01.01.2018.
- Male and female
- years or older
- Operated of supervised by a participating surgeon (participating in this study is not necessarily by a whole surgical department of a hospital, but by specific surgeons)
- Elective and emergency surgery
- Primary and recurrent hernia
- Metachronous and synchronous hernia
- Signed informed consent form
Exclusion Criteria4
- Younger than 18 years
- Not operated or supervised by participating surgeon
- Pregnant at inclusion in the registry
- No signed informed consent form
Interventions
DEVICESurgical inguinal or femoral hernia repair
Surgical inguinal or femoral hernia repair (primary or mesh)
Locations(2)
View Full Details on ClinicalTrials.gov
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NCT04623580