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NCT Number: NCT05516576

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

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.

Recruiting

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Chu Grenoble Alpes

La Tronche, 38043, France

Location status: Recruiting

Location contact

Anne-Laure BOREL, MDD

CONTACT

[email protected]

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

endomina®

Device

Endoscopic gastroplasty

Primary outcomes

  1. Remission of diabetes after endoscopic gastroplasty with endomina, in patients with type-2 diabetes and class I obesity

    Time frame: 24 months

    Remission is defined as HbA1c < 6.5% without antidiabetic drug for at least 3 months

Study contacts

Contact information is provided by the study sponsor or research team.

L. LECLERCQ, MSc

CONTACT

[email protected]

+3271919409

Sponsors and collaborators

Lead sponsor

University Hospital, Grenoble

Other

Collaborators

  • Endo Tools Therapeutics S.A.

Registry information

Acronym: ESTIME

Important dates

Study start
2023
Primary completion
2028
Study completion
2028
First posted
Aug 25, 2022
Registry last updated
Mar 14, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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