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Patient Reported Outcome Measures in Umbilical Hernia Surgery

StatusEnrolling by Invitation
PhaseNot specified
Started
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Record History

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  1. Trial sites expanded: 1 → 4 locations
    • Eligibility criteria shortened, about 3 words
    v2
  2. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
This study collects information on symptoms before and after elective umbilical hernia repair. Enrollment in the study does not alter the planned surgery. The goal is to better understand so called patient-reported outcome measures in umbilical hernia patients and actual patient reported outcomes will be compared to perceived hernia surgeon reported outcomes through an electronic questionnaire.
Trial Details
NCT Number NCT07717021
Lead Sponsor Blekinge County Council Hospital
Conditions
(from sponsor)		 Umbilical Hernia Repair
Related terms Chronic Pain
Enrollment 200 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov