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Glucose-homeostasis After Endoscopic Sleeve Gastroplasty

Primary Purpose

Obesity, Morbid

Status
Recruiting
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
Oral glucose tolerance test
Sponsored by
Insel Gruppe AG, University Hospital Bern
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Obesity, Morbid

Eligibility Criteria

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

Inclusion Criteria:

  • Planned ESG
  • Written informed consent
  • Male or female sex
  • Age 18-65 years
  • BMI ≥ 40 kg/m2 OR
  • BMI ≥ 35 kg/m2 and obesity-related comorbidities except type 2 diabetes

Exclusion Criteria:

  • Type 1 or Type 2 Diabetes
  • Type 2 Diabetes according to pathological OGTT at visit 2
  • Mandatory use of medical drugs that influence glucose metabolism
  • Participant had bariatric procedures other than ESG
  • Abdominal surgery influencing glucose metabolism
  • Moderate to severe chronic kidney, liver, or pancreatic disease
  • Pregnancy or breastfeeding
  • Physical or psychological disease likely to interfere with the normal conduct of the study and interpretation of the study results as judged by the investigator

Sites / Locations

  • Department of Diabetes, Endocrinology, Nutritional Medicine and Metabolism, Inselspital, Bern University Hospital, University of Bern, Bern, SwitzerlandRecruiting

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

All participants

Arm Description

Participants scheduled for endoscopic sleeve gastroplasty

Outcomes

Primary Outcome Measures

Area under the curve for plasma glucose in oral glucose tolerance test
Plasma glucose will be measured in oral glucose tolerance test following dapagliflozin and will be compared with concentrations measured following placebo. Active and inactivated glucagon like peptide I will be measured.

Secondary Outcome Measures

Area under the curve for glucagon-like peptide I in oral glucose tolerance test
Glucagon-like peptide I will be measured in oral glucose tolerance test following dapagliflozin and will be compared with concentrations measured following placebo. Active and inactivated glucagon like peptide I will be measured.
Area under the curve for gastric inhibitory peptide in oral glucose tolerance test
Gastric inhibitory peptide will be measured in oral glucose tolerance test following dapagliflozin and will be compared with concentrations measured following placebo. Active and inactivated glucagon like peptide I will be measured.
Area under the curve for glucagon in oral glucose tolerance test
Glucagon will be measured in oral glucose tolerance test
Area under the curve for somatostatin in oral glucose tolerance test
Somatostatin will be measured in oral glucose tolerance test
Area under the curve for non-acyl ghrelin in oral glucose tolerance test
Non-acyl Ghrelin will be measured in oral glucose tolerance test
Area under the curve for insulin in oral glucose tolerance test
Insulin will be measured in oral glucose tolerance test

Full Information

First Posted
August 19, 2019
Last Updated
November 7, 2022
Sponsor
Insel Gruppe AG, University Hospital Bern
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1. Study Identification

Unique Protocol Identification Number
NCT04063098
Brief Title
Glucose-homeostasis After Endoscopic Sleeve Gastroplasty
Official Title
Effects of Endoscopic Sleeve Gastroplasty on Hormonal Markers of Glucose-homeostasis
Study Type
Interventional

2. Study Status

Record Verification Date
November 2022
Overall Recruitment Status
Recruiting
Study Start Date
January 30, 2020 (Actual)
Primary Completion Date
June 30, 2024 (Anticipated)
Study Completion Date
July 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Insel Gruppe AG, University Hospital Bern

4. Oversight

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

5. Study Description

Brief Summary
Endoscopic sleeve gastroplasty (ESG) is a transoral endoscopic procedure that creates a tubular sleeve along the lesser curvature with a gastric volume of approximately 30%. Summarizing the available literature published since its introduction in 2013, ESG was capable to achieve > 10% of sustained total body weight loss in a majority of mildly to moderately obese patients with the caveat of only minor adverse events. Besides weight loss, little is known about the metabolic effects of ESG. The present study seeks to measure markers of glucose homeostasis during oral glucose tolerance tests before and subsequently after application of ESG in 12 patients.
Detailed Description
Endoscopic sleeve gastroplasty (ESG) is a transoral endoscopic procedure that utilizes full-thickness sutures extending from the prepyloric antrum to the gastroesophageal junction, creating a tubular sleeve along the lesser curvature with a gastric volume of approximately 30%. After the first feasibility study was available in 2013, multiple investigators published data on safety and efficacy of ESG. A recent meta analysis of novel endoscopic procedures revealed four observational studies on ESG. At 6, 12 and 24 months pooled excessive weight loss (EWL) was 52%, 53%, and 60% while pooled total body weight loss (TBWL) was 16%, 17%, and 20%, respectively. Aside from its efficacy in terms of body weight loss, only a small number of investigations addressed metabolic changes in response to ESG so far. In a large retrospective analysis, which observed the outcomes of 1000 patients following ESG, 13 of 17 cases of type 2 diabetes mellitus (T2DM), all 28 cases of hypertension, and 18 of 32 cases of dyslipidemia were in complete remission by the third month of follow-up. Summarizing the available literature, knowledge about effects of ESG on metabolism and glucose homeostasis is scarce. Available studies are subject to significant limitations in terms of sample size and or generalizability of results. The present study aims at a comprehensive determination of changes in hormonal regulators of glucose homeostasis after ESG in comparison to the preoperative state. Up to date, there are no structured and detailed analyses available that investigate glucose homeostasis following ESG. Proper glucose homeostasis yields a significant impact on a patients' quality of life and may - if deteriorated - be accompanied by a plethora of somatic and psychological constraints. The results of the present study seeks to investigate glucose homeostasis following ESG in detail. This may help to identify patients in need for further assistance regarding their post-interventional lifestyle in order to avoid e.g. hypoglycemia, and to further characterize patients' cohorts that will likely benefit from ESG.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity, Morbid

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
12 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
All participants
Arm Type
Other
Arm Description
Participants scheduled for endoscopic sleeve gastroplasty
Intervention Type
Other
Intervention Name(s)
Oral glucose tolerance test
Intervention Description
Oral glucose tolerance test (OGTT) after a 72-hours standardized diet. OGTT will be performed 1 month prior to as well as 1, 3, 6, and 12 months after endoscopic sleeve gastroplasty
Primary Outcome Measure Information:
Title
Area under the curve for plasma glucose in oral glucose tolerance test
Description
Plasma glucose will be measured in oral glucose tolerance test following dapagliflozin and will be compared with concentrations measured following placebo. Active and inactivated glucagon like peptide I will be measured.
Time Frame
From time-point 0 to 120 minutes during oral glucose tolerance test, measurement every 15 minutes
Secondary Outcome Measure Information:
Title
Area under the curve for glucagon-like peptide I in oral glucose tolerance test
Description
Glucagon-like peptide I will be measured in oral glucose tolerance test following dapagliflozin and will be compared with concentrations measured following placebo. Active and inactivated glucagon like peptide I will be measured.
Time Frame
From time-point 0 to 120 minutes during oral glucose tolerance test, measurement every 15 minutes
Title
Area under the curve for gastric inhibitory peptide in oral glucose tolerance test
Description
Gastric inhibitory peptide will be measured in oral glucose tolerance test following dapagliflozin and will be compared with concentrations measured following placebo. Active and inactivated glucagon like peptide I will be measured.
Time Frame
From time-point 0 to 120 minutes during oral glucose tolerance test, measurement every 15 minutes
Title
Area under the curve for glucagon in oral glucose tolerance test
Description
Glucagon will be measured in oral glucose tolerance test
Time Frame
From time-point 0 to 120 minutes during oral glucose tolerance test, measurement every 15 minutes
Title
Area under the curve for somatostatin in oral glucose tolerance test
Description
Somatostatin will be measured in oral glucose tolerance test
Time Frame
From time-point 0 to 120 minutes during oral glucose tolerance test, measurement every 15 minutes
Title
Area under the curve for non-acyl ghrelin in oral glucose tolerance test
Description
Non-acyl Ghrelin will be measured in oral glucose tolerance test
Time Frame
From time-point 0 to 120 minutes during oral glucose tolerance test, measurement every 15 minutes
Title
Area under the curve for insulin in oral glucose tolerance test
Description
Insulin will be measured in oral glucose tolerance test
Time Frame
From time-point 0 to 120 minutes during oral glucose tolerance test, measurement every 15 minutes

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: Planned ESG Written informed consent Male or female sex Age 18-65 years BMI ≥ 40 kg/m2 OR BMI ≥ 35 kg/m2 and obesity-related comorbidities except type 2 diabetes Exclusion Criteria: Type 1 or Type 2 Diabetes Type 2 Diabetes according to pathological OGTT at visit 2 Mandatory use of medical drugs that influence glucose metabolism Participant had bariatric procedures other than ESG Abdominal surgery influencing glucose metabolism Moderate to severe chronic kidney, liver, or pancreatic disease Pregnancy or breastfeeding Physical or psychological disease likely to interfere with the normal conduct of the study and interpretation of the study results as judged by the investigator
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Markus Laimer, Prof. MD
Phone
+41316323062
Ext
+41316323062
Email
Markus.Laimer@insel.ch
First Name & Middle Initial & Last Name or Official Title & Degree
Andreas Melmer, MD
Phone
+41316323062
Ext
+41316323062
Email
Andreas.Melmer@insel.ch
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Markus Laimer, Prof. MD
Organizational Affiliation
Department of Diabetes, Endocrinology, Clinical Nutrition and Metabolism, University Clinics Bern, Inselspital, Bern, Switzerland
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Diabetes, Endocrinology, Nutritional Medicine and Metabolism, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland
City
Bern
ZIP/Postal Code
3010
Country
Switzerland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Markus Laimer, Prof. MD
Phone
+41 31 63 2 30 62
Email
Markus.Laimer@insel.ch
First Name & Middle Initial & Last Name & Degree
Andreas Melmer, MD, PhD
Phone
+41 31 66 4 02 49
Email
Andreas.Melmer@insel.ch

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Time Frame
July 30th 2022
IPD Sharing Access Criteria
Contact with the Study Sponsor

Learn more about this trial

Glucose-homeostasis After Endoscopic Sleeve Gastroplasty

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