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Magnet surgery safety check: will new device reduce bowel blockages?

NCT ID NCT06928545

Knowledge-focused Sponsor: GT Metabolic Solutions, Inc. Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 25, 2026 · Last updated Sep 11, 2026 · Updated 3 times

Summary

This study follows 106 people who had weight-loss surgery using the MagDI system, a device that uses magnets to create a new connection between parts of the intestine. The main goal is to see how often internal hernias or bowel blockages happen within one year after surgery. Researchers will compare these results to earlier studies to check if the device is safe.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
MagDI System (magnetic device for creating intestinal connections)
What this could lead to
If successful, this registry could confirm that the MagDI system is as safe as traditional surgical methods for creating intestinal connections in weight-loss surgery.
What could go wrong
This is an observational registry, not a controlled trial, so it cannot prove the device causes or prevents complications. Results may not apply to all patients.

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

About 106 people

The number the study aims to enrol. It can still change while the study runs.

Started

Mar 2025

Expected to finish

Apr 2027

An estimate. End dates often move.

Lead sponsor

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

All eligible patients in the U.S. who undergo a side-to-side duodeno-ileal anastomosis with the MagDI System.

Ages

22 years and older

Sex

Anyone

Healthy volunteers

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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: 1. \>21 years of age, at the time of informed consent. 2. Body Mass Index (BMI) between 30-50 kg/m2. 3. Indicated for a side-to-side duodeno-ileal anastomosis and is treated with the MagDI System at a U.S. registry center. 4. Participant has been informed of the nature of the registry. Exclusion Criteria: 1\. Participant does not provide informed consent to be enrolled and followed in the registry.

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Conditions

The condition(s) this trial relates to.

Internal Hernia intestinal obstruction obesity disorder

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Anastomosis, surgical Bowel obstruction Internal hernia

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The study's own enquiry address

    This study publishes an address for enquiries. See it below .

  2. The places running it

    6 sites. The list below names each one and where it is.

  3. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  4. 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

Study contacts

  • Contact

    Email: •••••@•••••

  • Contact

    Email: •••••@•••••

Locations

  • Baptist Healthcare System, Inc.

    RECRUITING

    Louisville, Kentucky, 40299, United States

  • Bariatric Specialists of the Carolinas

    RECRUITING

    Cary, North Carolina, 27518, United States

  • HCA Florida Mercy

    RECRUITING

    Miami, Florida, 33133, United States

  • Ochsner Clinic Foundation

    RECRUITING

    Lafayette, Louisiana, 70503, United States

  • Transform Weight Loss

    RECRUITING

    Lynnwood, Washington, 98036, United States

  • Ventura Advanced Surgical Associates

    RECRUITING

    Ventura, California, 93003, United States

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