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MagDI U.S. Registry

Post-Market Assessment of the Incidence and Severity of Internal Hernia and Bowel Obstruction at One Year Following Use of the MagDI System to Create Side-to-Side Duodeno-Ileal Magnetic Compression Anastomoses (MagDI US Registry)

Who can join

Ages 22 and older · All sexes

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.

About the study

Assess the incidence and severity of internal hernia and bowel obstruction at one year in a U.S. population following use of the MagDI System to create side-to-side duodeno-ileal anastomoses.

What is being tested

• Side-to-side duodenal-ileal anastomosis (device)

Sponsor: GT Metabolic Solutions, Inc. · Participants: 106 · Started: Mar 28, 2025

Contact the study team

• Lisa Griffin Vincent, PhD, MA · Phone: +1 763-200-1416
• Josh Schumacher · Phone: +1 763-200-1416

Official record on ClinicalTrials.gov — NCT06928545

Locations in the U.S.

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.