Magnetic ring for heartburn tracked for 10 years
NCT ID NCT04253392
First seen Jun 25, 2026 · Last updated Aug 28, 2026 · Updated 4 times
Summary
This registry follows 500 adults who receive the LINX device, a ring of magnetic beads implanted around the esophagus to help keep stomach acid down. The goal is to check for safety issues like device movement, erosion, or swallowing problems over up to 10 years. Participants will also report how their reflux symptoms and quality of life change.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- LINX Reflux Management System (magnetic bead ring implanted around the esophagus)
- What this could lead to
- If successful, this registry will confirm that the LINX device is safe and effective for controlling GERD over the long term, helping patients avoid daily medication.
- What could go wrong
- This is an observational registry, not a controlled trial, so it cannot prove the device works better than other treatments. Risks include device erosion, migration, or need for removal.
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.
- Participants
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500 people
The number who actually took part.
- Started
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Jul 2020
- Expected to finish
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Jul 2032
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Adult patients successfully implanted (treated) with the LINX Reflux Management System for the treatment of GERD (Implant success defined as leaving the surgical suite with a device in situ)
- Ages
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21 to 99 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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: 1. Subject is \>or=21 years old 2. Subject with prospective plans for a LINX procedure 3. Subject provides written informed consent 4. Subject must be willing and able to complete questionnaires/ surveys electronically (ePROs) Exclusion Criteria: 1. Subject who was previously implanted with LINX device 2. Any reason which the Principal Investigator believes may cause the subject to be non-compliant with or unable to meet the protocol requirements (i.e. medical illness and/or limited life expectancy of less than 10 years) Note: Physicians should refer to the LINX Reflux Management System IFU for a complete list of contraindications, warnings, and precautions.
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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.
Contacts and locations
Locations
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Adv Surg Assoc / Self Regional Healthcare
Greenwood, South Carolina, 29646, United States
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Bariatric Medical Institute of Texas
San Antonio, Texas, 78258, United States
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East Carolina University / Vidant Medical Center
Greenville, North Carolina, 27834, United States
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Epsom Hospital
Epsom, KT18 7EG, United Kingdom
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Fox Valley Surgical Associates
Appleton, Wisconsin, 54911, United States
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Gen Surg Assoc / Fairfield Medical Center
Lancaster, Ohio, 43130, United States
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Guy's and St. Thomas' Hospitals
London, SE1 7EH, United Kingdom
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Houston Methodist
Houston, Texas, 77030, United States
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Institute of Esophageal and Reflux Surgery
Englewood, Colorado, 80113, United States
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Keck Hospital of USC
Los Angeles, California, 90033, United States
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Lehigh Valley Hospital - Cedar Crest
Allentown, Pennsylvania, 18102, United States
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Lexington Surgery
West Columbia, South Carolina, 29169, United States
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Marien Hospital Herne
Herne, 44625, Germany
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MedUni Wien / Universitatsklinik fur Chirurgie
Vienna, 1090, Austria
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Minimal Access Surgery/Prisma Health - Upstate
Greenville, South Carolina, 29607, United States
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NW Allied Bariatric and Foregut Surgery
Tucson, Arizona, 85741, United States
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National University Hospital
Singapore, 119228, Singapore
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OSF Medical Group
Peoria, Illinois, 61615, United States
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Panhandle Weight Loss Center
Amarillo, Texas, 79106, United States
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RefluxUK
Royal Tunbridge Wells, TN3 0RD, United Kingdom
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Richmond Surg / Henrico Doctors' Hospital
Richmond, Virginia, 23229, United States
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Saint Elizabeth Healthcare Edgewood
Edgewood, Kentucky, 41017, United States
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Sparrow Hospital / Sparrow Medical Group
Lansing, Michigan, 48912, United States
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Swedish Medical Center
Seattle, Washington, 98104, United States
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The Ohio State University
Columbus, Ohio, 43210, United States
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Univ of Milano / IRCCS Policlinico San Donato
San Donato Milanese, 20097, Italy
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University of South Alabama
Mobile, Alabama, 36617, United States
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University of Southern Florida (Tampa General Hospital)
Tampa, Florida, 33606, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Which acid blocker wins in obese reflux patients?
- Through-the-Mouth surgery vs keyhole surgery: which works better for a rare swallowing disorder?
- Zapping the esophagus: an implantable device takes on chronic heartburn
- Feeding into the small intestine may reduce reflux and oxygen dips in fragile preterm infants
- Unnecessary test? study questions routine throat tube before reflux surgery
- Could stomach surgery raise cancer risk? new study investigates