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Terminated Not applicable Interventional

SEAM Trial: Sutureless End to End Anastomosis by Magnetic Compression

ClinicalTrials.gov ID: NCT05046730

Public ClinicalTrials.gov record NCT05046730. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 17, 2026, 6:48 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

SEAM Trial: Sutureless End to End Anastomosis by Magnetic Compression: A Study to Evaluate Safety and Effectiveness of Self-Forming Magnet (SFM) Anastomosis Device: A Historically Controlled Propensity Matched Study

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The objectives of this study are to determine the safety and effectiveness of the SFM Anastomosis Device when used to create a small bowel anastomosis for patients undergoing ileostomy reversal as compared with a propensity-matched historic control group of patients who underwent ileostomy reversal using a conventional closure technique (sutures or stapler).

Study identification

NCT ID
NCT05046730
Recruitment status
Terminated
Study type
Interventional
Phase
Not applicable
Lead sponsor
GI Windows, Inc.
Industry
Enrollment
128 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 1, 2022 (Actual)
Primary completion
Oct 1, 2023 (Actual)
Completion
Dec 30, 2023 (Actual)
Last update posted
Oct 15, 2024

2022 – 2023

United States locations

U.S. sites
14
U.S. states
10
U.S. cities
13
Facility City State ZIP Site status
Advent Health Orlando Florida 32803 —
Colon and Rectal Clinical of Orlando Orlando Florida 32806 —
Beth Israel Deaconess Medical Center Boston Massachusetts 02215 —
University of Massachusetts Medical School Worcester Massachusetts 01655 —
Spectrum Health / Ferguson Clinic Grand Rapids Michigan 49508 —
Trinity Health Michigan Heart Ypsilanti Michigan 48197 —
Dartmouth Hitchcock Medical Center Lebanon New Hampshire 03766 —
The Mount Sinai Medical Center New York New York 10029 —
St Francis Hospital Roslyn New York 11576 —
Novant Health Clinical Research Winston-Salem North Carolina 27101 —
Penn State Milton S. Hershey Medical Center Hershey Pennsylvania 17033 —
Vanderbilt University Medical Center Nashville Tennessee 37232 —
UT Health Science Center at Houston Houston Texas 77030 —
The Medical College of Wisconsin Milwaukee Wisconsin 53226 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05046730, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 15, 2024 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05046730 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →