Impact of Biosynthetic Mesh on Paraesophageal Hernia Repair
Weill Medical College of Cornell University · with Intuitive Surgical · NCT06444347
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18+ · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Not applicable
- Target enrollment
- 200
- US sites recruiting
- 1
- Study start
- June 10, 2024
- Record last updated
- August 19, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
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.
Being studied: Biosynthetic Mesh; Hiatal Hernia Repair
Conditions: Hiatal Hernia
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full 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
Recruiting US locations
Weill Cornell Medicine
New York, NY 10065
Site contact: Annabel Endean, NP · 646-962-5250 · ant2028@med.cornell.edu
Study contacts (from the official record)
- Annabel Endean, NP · 646-962-5250 · ant2028@med.cornell.edu
- Niloufar Salehi, MD · nis4017@med.cornell.edu
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