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Clinical Trials in France / NCT05516576
Recruiting Not applicable

Endoscopic Sutured Gastroplasty with Endomina® Device Versus Standard of Care in Patients with Type 2 Diabetes and Class I Obesity: a Multi-center, Randomized Controlled Trial

NCT05516576 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2023-09-29
Last updated
2025-03-14

Condition(s) studied

Diabetes Mellitus, Type 2Obesity

Investigational drug(s) / intervention(s)

endomina®

endomina®: Endoscopic gastroplasty

Study summary

The primary objective of this study is to assess the efficacy of endoscopic gastric reduction with the endomina® device, in combination with standard of care, compared to standard of care alone, on the remission of diabetes 24 months after surgery, in patients with type-2 diabetes and class I obesity.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * Age between 18-65 years; * Recently diagnosed Type 2 Diabetes (\<= 10 years): * HbA1c \< 9%: * Under non-insulin anti-diabetic treatment, i.e., metformin, sulfonylurea, glinide, DPP4i, GLP1-RA, SGLT2i, alone or in combination * Anti-diabetic therapy stable during the last 3 months before inclusion * BMI between 30-34.9 kg/m² with adaptation for Asian population 27.5-32.5kg/m² * Must be able to comply with all study requirements for the duration of the study as outlined in the protocol (including compliance to randomization treatment, dietary follow up, visits schedule and all study specific procedures); * Must be able to understand and be willing to provide written informed consent. Exclusion Criteria: * Contra-indication to the use of endomina® and TAPES according to their Instruction for Use (IFU). * Type I diabetes characterized by C peptide \<0.2 nmol/l or presence of anti-GAD, anti IA2, anti-ZNT8 * Unstable diabetic retinopathy * Severe kidney (stage 4-5), hepatic (child B and C cirrhosis), pulmonary disease or cancer (cancer in the past 5 years); * Short-term prognosis due to a proven serious comorbidity including severe macrovascular complications and / or a limited life expectancy (\<5 years) * Contra-indication to endoscopic gastroplasty (...) * Impending gastric surgery 60 days post intervention; * Participant involved in another interventional clinical study * Patients having alcoholic or drug addiction; * Patients having a severe mental illness such as psychosis, bipolar disorders, severe, current depression or eating disorder such as bulimia nervosa or binge eating disorder; * Person deprived of liberty by judicial order * Person under guardianship or curatorship

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Chu Grenoble Alpes La Tronche France Recruiting

More University Hospital, Grenoble trials in France

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05516576 on ClinicalTrials.gov ↗ ← All trials in France