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NCT06928545 · ClinicalTrials.gov registry record

MagDI U.S. Registry

A clinical trial of Internal Hernia and Anastomosis, Surgical, sponsored by GT Metabolic Solutions.

Recruiting
Registry status
106
Enrollment target
5
Study locations

NCT06928545 is a study of Internal Hernia and Anastomosis, Surgical that is actively recruiting participants, run by GT Metabolic Solutions. The registered enrollment target is 106 participants. The trial reports 5 study locations across 5 states.

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The verdict

NCT06928545, a study of Internal Hernia and Anastomosis, Surgical, is actively recruiting participants, sponsored by GT Metabolic Solutions.

RECRUITING
Registry status
106 participants
Enrollment target
5
Study locations

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

What the Registry Record Tells You About NCT06928545

The ClinicalTrials.gov registry entry for NCT06928545 describes a study currently listed as recruiting, categorized as an unspecified phase. 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.

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.

NCT06928545 reports 5 study locations spanning 5 distinct geographic areas - top geographies include California, Kentucky, Louisiana.

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.

What interventions are being tested in trial NCT06928545?

The interventions under investigation include: Side-to-side duodenal-ileal anastomosis (DEVICE).

Who is sponsoring clinical trial NCT06928545?

This trial is sponsored by GT Metabolic Solutions, which has 1 total clinical trials registered on ClinicalTrials.gov.

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.

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

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