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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

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

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05516576
Acronym
ESTIME
Enrollment
200
Registered
2022-08-25
Start date
2023-09-29
Completion date
2028-12-31
Last updated
2025-03-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetes Mellitus, Type 2, Obesity

Brief 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.

Interventions

Endoscopic gastroplasty

Sponsors

Endo Tools Therapeutics S.A.
CollaboratorINDUSTRY
University Hospital, Grenoble
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 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

Design outcomes

Primary

MeasureTime frameDescription
Remission of diabetes after endoscopic gastroplasty with endomina, in patients with type-2 diabetes and class I obesity24 monthsRemission is defined as HbA1c \< 6.5% without antidiabetic drug for at least 3 months

Countries

France

Contacts

Primary ContactL. LECLERCQ, MSc
ESTIME@endotools.be+3271919409

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026