MagDI U.S. Registry for Surgical Anastomosis
This study, called the MagDI U.S. Registry, is looking at people who have had a specific type of surgery using the MagDI System. The MagDI System helps create a connection between the small intestine and the first part of the small intestine (a side-to-side duodenal-ileal anastomosis) using magnetic compression. The main goal is to see how often patients develop internal hernias or blockages in their bowels (bowel obstructions) within one year after this surgery. You might be able to join if you are over 21, have a BMI between 30 and 50, and are having this specific surgery with the MagDI System at a participating U.S. center. This is an observational study, meaning researchers will collect information about your health after the procedure.
- Study design
- This is an observational study planning to enroll 106 participants. It is designed to collect real-world information about patients who have undergone a specific surgical procedure.
- What's involved
- Not specified in the trial record.
- Compensation
- Not stated in the trial record.
- Follow-up
- Participants will be followed for the incidence of internal hernia and bowel obstructions for 360 days after their procedure.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
MagDI U.S. Registry
At a glance
Conditions
Where it's being run
5 sites across 5 statesWho to contact
Opens a ready-to-send draft in your own email app — review before sending.
What this trial measures
- Incidence of Internal Hernia and Bowel ObstructionsFrom date of study index procedure through 360 days.
To assess and characterize incidence and severity of internal hernia and bowel obstruction at one year in U.S. patients treated with the MagDI System compared with the pre-market study (GTM-001) and scientific literature.