MagDI Canada Study

GT Metabolic Solutions

Status

Enrolling

Conditions

Obesity

Type 2 Diabetes

Treatments

Device: Magnet System, DI Biofragmentable

Study type

Interventional

Funder types

Industry

Identifiers

NCT06467955

GTM-006

Details and patient eligibility

About

The objective of the MagDI Canada study is to evaluate the performance and safety of the MagDI System in eligible participants who are indicated for a duodeno-ileal (small bowel) side-to-side anastomosis procedure for partial intestinal diversion as one example of a small bowel clinical procedure requiring a side-to-side anastomosis. The secondary objective includes initial efficacy of the duodeno-ileal diversion using the MagDI System.

Full description

The partial diversion of intestinal contents from the duodenum to the ileum via side-to-side duodeno-ileostomy is intended to facilitate weight management / loss in obese adults and improve metabolic outcomes in obese adults with type 2 diabetes mellitus (T2DM). Side-to-side anastomoses are currently created by sutures, staples, and anastomotic compression devices. The most common side-to-side anastomosis technique used today is stapling, requiring cutting of the intestines and staples remain behind in the body. Linear staplers are available in different sizes (e.g., 30mm, 45mm, 50mm, 60mm). A predicate for this side-to-side duodeno-ileostomy diversion procedure is the single-anastomosis duodeno-ileostomy (SADI) procedure.

Enrollment

60 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Between 18-65 years of age, at the time of informed consent.
Body Mass Index (BMI) between 30-50 kg/m2
Meets one of the following criteria:
1. Type 2 Diabetes Mellitus (T2DM; defined as HbA1c ≥ 6.5%) or weight regain following previous sleeve gastrectomy (≥ 12 months); OR
2. Type 2 Diabetes Mellitus (T2DM; defined as HbA1c ≥ 6.5%) or weight regain following previous endoscopic sleeve gastroplasty (≥ 12 months); OR
3. Type 2 Diabetes Mellitus (defined as HbA1c ≥ 6.5%) with a Body Mass Index between 30-35 and without previous sleeve gastrectomy and no plan to perform a concurrent sleeve gastrectomy.
Participant agrees to refrain from any type of additional bariatric or reconstructive surgery that would affect body weight for the duration of the study.
Participant has been informed of the nature of the study and agrees to its provisions, complying with study required testing, medications, follow-up visits, and has provided written informed consent.

Exclusion criteria

Type 1 diabetes.
Use of injectable insulin.
Uncontrolled Type 2 Diabetes Mellitus (T2DM).
Investigator plans to perform a sleeve gastrectomy with the duodeno-ileal anastomosis procedure.
Uncontrolled hypertension, dyslipidemia or sleep apnea.
Prior intestinal, colonic or duodenal surgery (other than bariatric).
Prior surgery, trauma, prostheses, disease or genetic expression which prevent or contraindicate the procedure, including scarring and abnormal anatomy.
Refractory gastro-esophageal reflux disease (GERD).
Barrett's disease.
Helicobacter pylori positive and/or active ulcer disease.
Large hiatal hernia.
Inflammatory bowel or colonic diverticulitis disease.
Any anomaly precluding orogastric access by gastroscope and catheters, and manipulation techniques.
Any anomaly preventing / contraindicating endoscopic or laparoscopic access and procedures.
Implantable pacemaker or defibrillator.
Psychiatric disorder, except well-controlled depression with medication for > 6 months.
History of substance abuse.
Pregnant, lactating, or planning pregnancy during the clinical investigation. Note: Female participants of childbearing age must agree to use safe contraception (e.g., intrauterine devices, hormonal contraceptives: contraceptive pills, implants, transdermal patches hormonal vaginal devices, injections with prolonged release).
Any comorbidity or current status of participant's physiological fitness that in the surgeon's or anesthesiologist's opinion represents safety concerns that make the participant medically unfit for the procedure, including any significant congenital or acquired anomalies of the GI tract at or distal to the placement of the Magnets.
Unhealed ulcers, bleeding lesions, tumor, or any other lesion at target Magnet deployment site.
Expected need for Magnetic Resonance Imaging (MRI) within the first 2 months post-procedure.
Any surgical or interventional procedure (including planned and/or scheduled) within the period of 30 days prior to and 30 days following the study procedure.
Any stroke / Transient Ischemic Attack (TIA) 6 months prior to consent.
Requires chronic anticoagulation therapy (except aspirin).
Active infections requiring antibiotic therapy, unless resolved before undergoing the study procedure.
Recent tobacco or nicotine product cessation 3 months prior to informed consent.
Known allergies to the device components (including the biofragmentable material PGLA or similar compounds) or contrast media.
Participants with comorbidities that are likely to result in a life expectancy of 12 months.
Currently participating in an investigational drug or another device study that has not reached its primary endpoint: Note: Studies requiring extended follow-up for products that were investigational, but have since become commercially available, are not considered investigational trials.
A positive COVID-19 test prior to the study procedure in accordance with local COVID-19 protocol.
Presence of other anatomic or comorbid conditions, or other medical, social or psychological conditions that, in the investigator's opinion, could limit the participant's ability to participate in the clinical investigation or to comply with follow-up requirements, or impact the scientific soundness of the clinical investigation results.