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Impact of Biosynthetic Mesh on Paraesophageal Hernia Repair
The Impact of Biosynthetic Mesh on Paraesophageal Hernia Repair in Robotic Anti-Reflux Surgery: A Multi-Institutional Randomized Trial
Who can join
Ages 18 and older · All sexes · Healthy volunteers welcome
Full eligibility criteria
Inclusion Criteria: * Documented diagnosis of gastroesophageal reflux disease * Adults aged 18 years or older * English speaking * Subject is planned to undergo surgery for reflux disease Exclusion Criteria: * Physician deems the subject is unable to complete the study due to documented dementia. * Subject is undergoing emergent surgery. * Pregnancy * Patient has known allergy to tetracycline hydrochloride or kanamycin sulfate
About the study
The aim of this study is to find out if using a certain kind of mesh can reduce the chances of hiatal hernias coming back after anti-reflux surgery. Participants undergoing antireflux surgery will be assigned to one of two groups, a group that has surgery with mesh, or a group that has surgery without mesh.
What is being tested
- Biosynthetic Mesh (device)
- Hiatal Hernia Repair (procedure)
Sponsor: Weill Medical College of Cornell University · Participants: 200 · Started: Jun 10, 2024
Contact the study team
- Annabel Endean, NP · Phone: 646-962-5250
Official record on ClinicalTrials.gov — NCT06444347
Locations in the U.S.
| New York | Lenox Hill Hospital, New York (Not yet recruiting) NYU Langone Health, New York (Not yet recruiting) Weill Cornell Medicine, New York |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.