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RECRUITING

MagDI U.S. Registry

NCT06928545 · View on ClinicalTrials.gov ↗

Study Summary

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.

Interventions

  • DEVICE Side-to-side duodenal-ileal anastomosis

Study Locations (5)

California

  • Ventura Advanced Surgical Associates — Ventura

Kentucky

  • Baptist Healthcare System, Inc. — Louisville

Louisiana

  • Ochsner Clinic Foundation — Lafayette

North Carolina

  • Bariatric Specialists of the Carolinas — Cary

Washington

  • Transform Weight Loss — Lynnwood

Trial Details

FieldValue
Enrollment Target 106 participants
Start Date 2025-03-28
Est. Completion 2027-04

Sponsor

GT Metabolic Solutions

1 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06928545

The ClinicalTrials.gov registry entry for NCT06928545 describes a study currently listed as recruiting. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 106 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is GT Metabolic Solutions, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 3 conditions, with Internal Hernia appearing as the primary indexed condition, and to 1 intervention — of which Side-to-side duodenal-ileal anastomosis is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06928545 reports 5 study locations spanning 5 distinct geographic areas — top geographies include California, Kentucky, Louisiana. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06928545 about?

NCT06928545 is a clinical study titled "MagDI U.S. Registry". 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 the current status of trial NCT06928545?

This trial is currently recruiting. The enrollment target is 106 participants. The study started on 2025-03-28. Estimated completion is 2027-04.

What conditions does trial NCT06928545 study?

This clinical trial studies the following conditions: Internal Hernia, Anastomosis, Surgical, Bowel Obstruction. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06928545?

The interventions under investigation include: Side-to-side duodenal-ileal anastomosis (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06928545?

This trial is sponsored by GT Metabolic Solutions, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06928545 being conducted?

This trial has 5 study locations across California, Kentucky, Louisiana, North Carolina, Washington. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial