MagDI U.S. Registry

Recruiting now

Conditions studied: Anastomosis, Surgical, Internal Hernia, Bowel Obstruction

In brief

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.

Key facts

Study ID

NCT06928545

Run by

GT Metabolic Solutions, Inc.

People needed

106

Starts

2025-03-28

Expected to finish

2027-04-01

Last updated by the study team

2026-02-20

Who can join

Age: 22 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• >21 years of age, at the time of informed consent.
• Body Mass Index (BMI) between 30-50 kg/m2.
• Indicated for a side-to-side duodeno-ileal anastomosis and is treated with the MagDI System at a U.S. registry center.
• Participant has been informed of the nature of the registry.

You may not qualify if…

• Participant does not provide informed consent to be enrolled and followed in the registry.

Where it is running

• Ventura Advanced Surgical Associates — Ventura, California, United States (enrolling)
• Baptist Healthcare System, Inc. — Louisville, Kentucky, United States (enrolling)
• Ochsner Clinic Foundation — Lafayette, Louisiana, United States (enrolling)
• Bariatric Specialists of the Carolinas — Cary, North Carolina, United States (enrolling)
• Transform Weight Loss — Lynnwood, Washington, United States (enrolling)

Full record on ClinicalTrials.gov

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