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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 (ESTIME)

Primary Purpose

Diabetes Mellitus, Type 2, Obesity

Status
Recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
endomina®
Sponsored by
University Hospital, Grenoble
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetes Mellitus, Type 2

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age between 18-65 years;
  • Recently diagnosed Type 2 Diabetes (< 8 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

Sites / Locations

  • Chu Grenoble AlpesRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

endoscopic gastroplasty with endomina®

control

Arm Description

Outcomes

Primary Outcome Measures

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

Secondary Outcome Measures

Full Information

First Posted
July 15, 2022
Last Updated
October 2, 2023
Sponsor
University Hospital, Grenoble
Collaborators
Endo Tools Therapeutics S.A.
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1. Study Identification

Unique Protocol Identification Number
NCT05516576
Brief Title
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
Acronym
ESTIME
Official Title
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
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Recruiting
Study Start Date
September 29, 2023 (Actual)
Primary Completion Date
March 2024 (Anticipated)
Study Completion Date
December 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Grenoble
Collaborators
Endo Tools Therapeutics S.A.

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Type 2, Obesity

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
200 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
endoscopic gastroplasty with endomina®
Arm Type
Experimental
Arm Title
control
Arm Type
No Intervention
Intervention Type
Device
Intervention Name(s)
endomina®
Intervention Description
Endoscopic gastroplasty
Primary Outcome Measure Information:
Title
Remission of diabetes after endoscopic gastroplasty with endomina, in patients with type-2 diabetes and class I obesity
Description
Remission is defined as HbA1c < 6.5% without antidiabetic drug for at least 3 months
Time Frame
24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age between 18-65 years; Recently diagnosed Type 2 Diabetes (< 8 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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Loulia LECLERCQ, PhD
Phone
+32499532030
Email
loulia.leclercq@endotools.be
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anne-Laure BOREL, MD PHD
Organizational Affiliation
University Grenoble Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Chu Grenoble Alpes
City
La Tronche
ZIP/Postal Code
38043
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Anne-Laure BOREL, MDD
Email
ALBorel@chu-grenoble.fr

12. IPD Sharing Statement

Plan to Share IPD
Undecided

Learn more about this 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

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