NCT05807763
Fundoplication in Laparoscopic PEH Repair Based on FLIP
Enrolling by Invitation
NAAges 18+InterventionalTreatmentThe Foundation for Surgical Innovation and EducationInvestigator-initiated
~260 participants
Updated 2024-11-27 on ClinicalTrials.gov
What's tested:Laparoscopic paraesophageal hernia repair without fundoplication
At a glance
Recruiting sites
0 of 2 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Number of participants with GERD post-op
Measured over 12 months
Conditions
Where it's being run
2 sites across 2 statesIllinois1
Oregon1
Study leadership
- Christy M Dunst, MD · PRINCIPAL_INVESTIGATOR · The Oregon Clinic
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
Do you actually qualify for this trial?
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Eligibility criteria
Inclusion
Patients undergoing laparoscopic paraesophageal hernia repair
Exclusion
History of a prior hiatal hernia/paraesophageal hernia repair
Patients with objective GERD preoperatively
Intra-operative short esophagus
Defective gastroesophageal reflux barrier as determined by impedance planimetry (FLIP)
Defective gastroesophageal reflux barrier as determined by intra-operative endoscopy
What this trial measures
- Number of participants with GERD post-op12 months
Patients will undergo endoscopic evaluation and 48 hour pH testing to determine the incidence of objective GERD with and without fundoplication after PEH repair.