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Impact of Biosynthetic Mesh on Paraesophageal Hernia Repair

Weill Medical College of Cornell University · with Intuitive Surgical · NCT06444347

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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
Impact of Biosynthetic Mesh on Paraesophageal Hernia Repair (NCT06444347) | Bored Studies