Aleman Hospital
Buenos Aires, C1118AAT, Argentina
NCT Number: NCT03130244
Study will monitor changes in HbA1c for subjects in Intervention arm vs control arm.
This study is active but is not currently recruiting participants.
18 year–65 year
All sexes
Interventional
Not applicable
Buenos Aires, C1118AAT, Argentina
Randomized, Single-Center, Parallel-group, Open-label Pilot Study to Evaluate the Safety and Effectiveness of the GI Windows Magnet Anastomosis System (MAS) When Used to Create a Dual-path Enteral Diversion Compared with Medical Therapy Alone To Effect Glycemic Control in Obese Patients with Type 2 Diabetes Mellitus (T2DM)
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The MAS will be placed using an endoscope in the duodenum and and laparoscopically into ileum. A compression anastomosis will be created in each of the patients and the diversion of enteral flow from the duodenum to ileum treats Type 2 diabetes.
Other names: MAS
The best medical management for the patients in this arm will be decided by the endocrinologist based on protocol parameters.
Other names: No other intervention
Time frame: 12 months
The primary effectiveness endpoint is Mean change in HbA1c from baseline
Time frame: 12 months
12 month weight loss measured as a percent of total body weight loss and excess weight loss (using the BMI method) as well as weight/BMI change from baseline
Time frame: 12 months
Proportion of subjects experiencing diabetes remission and/or partial remission at 12 months (as defined by the American Diabetes Association)
Time frame: 12 months
Change in diabetes medication requirements from baseline to 12 months
GI Windows, Inc.
Industry
A Trial for a Procedure for Duodenum to Ileal Diversion to Treat Type 2 Diabetes
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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