← Back to Clinical Trials
Recruiting NCT06193551

Ovitex in Paraesophageal and Large Hiatal Hernia Repair

Trial Parameters

Condition Paraesophageal Hernia
Sponsor Foregut Research Foundation
Study Type INTERVENTIONAL
Phase N/A
Enrollment 100
Sex ALL
Min Age 18 Years
Max Age 85 Years
Start Date 2024-02-19
Completion 2030-01
Interventions
Ovitex LPR

Brief Summary

The purpose of the study is to evaluate the success of hiatal hernia repairs in patients with large (\>5cm) or paraesophageal hernias when Ovitex LPR mesh used during the repair.

Eligibility Criteria

Inclusion Criteria: * 18-85 year old with PEH and appropriate surgical indication for repair Exclusion Criteria: * Under 22 years of age. * In need of an emergency procedure. * Currently being treated with another investigational drug or device. * Have had prior gastric or esophageal surgery. * Have had any previous intervention for GERD. * Are suspected or confirmed to have esophageal or gastric cancer. * Have a Body Mass Index (BMI) greater than 45. * Cannot understand trial requirements or are unable to comply with follow-up schedule. * Are pregnant, nursing, or plan to become pregnant. * Have a mental health disorder that would interfere with your ability to follow study instructions. * Have suspected or known allergies to Ovitex * Have an illness that may cause you to be unable to meet the protocol requirements or is associated with shortened life expectancy.

Related Trials