Fundoplication in Laparoscopic PEH Repair Based on FLIP

Enrolling by invitation · Not applicable

Conditions studied: Paraesophageal Hernia

In brief

Prospective randomized controlled trial to identify a sub-set of patients that do not benefit from the routine addition, and added morbidity, of a fundoplication during laparoscopic paraesophageal hernia repair.

Key facts

Study ID

NCT05807763

Run by

The Foundation for Surgical Innovation and Education

People needed

260

Starts

2023-02-22

Expected to finish

2029-02-22

Last updated by the study team

2024-11-27

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Patients undergoing laparoscopic paraesophageal hernia repair

You may not qualify if…

• 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

Where it is running

• NorthShore University HealthSystem — Evanston, Illinois, United States
• Providence Portland Medical Center / The Oregon Clinic — Portland, Oregon, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.