Mesh may keep hernias away after reflux surgery
NCT ID NCT06444347
First seen Jun 27, 2026 · Last updated Aug 20, 2026 · Updated 2 times
Summary
This study looks at whether using a biosynthetic mesh during robotic anti-reflux surgery can lower the chance that a hiatal hernia returns. About 200 adults with GERD who are already scheduled for surgery will be randomly assigned to receive either the standard repair or repair with the mesh. The main goal is to see if the mesh helps keep the hernia from coming back.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 200 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jun 2024
- Expected to finish
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Jul 2030
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
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
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
3 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Lenox Hill Hospital
NOT_YET_RECRUITINGNew York, New York, 10075, United States
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Louisiana State University School of Medicine
WITHDRAWNNew Orleans, Louisiana, 70112, United States
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NYU Langone Health
NOT_YET_RECRUITINGNew York, New York, 10016, United States
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University of Southern California Keck School of Medicine
WITHDRAWNLos Angeles, California, 90089, United States
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Washington University School of Medicine
WITHDRAWNSt Louis, Missouri, 63110, United States
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Weill Cornell Medicine
RECRUITINGNew York, New York, 10065, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can a radiofrequency zap calm stubborn heartburn?
- Can a Pre-Surgery checklist predict who will still have reflux after fundoplication?
- Can a less invasive reflux surgery match the standard one?
- Can thread acupuncture boost GERD relief beyond standard pills?
- A Super-Microscope could spot acid reflux in Kids—Without guesswork?
- Could a tailored diet quiet the burn of acid reflux?