Flemish Inguinal and Femoral Hernia Prospective Registry
ConditionInguinal Hernia
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversitaire Ziekenhuizen KU Leuven
About this trial
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 criteria
Qualifiers
Consecutively all patients with a groin hernia (inguinal and/or femoral hernia) operated starting 01.01.2018.
Male and female
18 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)
Disqualifiers
Younger than 18 years
Not operated or supervised by participating surgeon
Pregnant at inclusion in the registry
No signed informed consent form
Trial design
Treatments tested in this trial
- Surgical inguinal or femoral hernia repair
Treatment groups
560 Participants
are divided into 1 treatment groupSponsors and collaborators
Source ClinicalTrials.gov