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The Importance of Ghrelin for Glucose Metabolism After Sleeve Gastrectomy

Primary Purpose

Bariatric Surgery Candidate, Glucose Metabolism Disorders

Status
Recruiting
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Ghrelin
Placebo
Sponsored by
Hvidovre University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Bariatric Surgery Candidate focused on measuring Ghrelin, Gastric sleeve, Glucose metabolism

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Sleeve gastrectomy-operated > 12 months prior to inclusion
  • Weight stable (+/- 3 kg during the last 3 months)
  • Fasting glucose < 7,0 mmol/l / HbA1c < 48 mmol/mol pre- and postoperative
  • Signed written informed consent

Exclusion Criteria:

  • Pregnancy or breastfeeding.
  • Haemoglobin < 6,5 mM.

Sites / Locations

  • Hvidovre Universitets HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Gastric sleeve operated

Matched control group

Arm Description

12 subjects with normal glucose tolerance (NGT) operated with SG minimum 12 month earlier

12 weight-matched unoperated subjects with NGT

Outcomes

Primary Outcome Measures

The difference in disposition index between the two study days with and without ghrelin in fusion in the SG operated group
The first phase insulin response will be related to the ambient insulin sensitivity by calculating the disposition index (FPIR x M-value).

Secondary Outcome Measures

The difference in first phase insulin response (FPIR) between the two study days with and without ghrelin in fusion in the SG operated group
Estimation of beta-cell function, calculated from insulin secretion rate using c-peptid and deconvolution from 0-10 min.
The difference in Insulin sensitivity (M-value) between the two study days with and without ghrelin in fusion in the SG operated group
When a steady state is reached at the end of the clamp, the glucose infusion rate represents insulin-mediated glucose uptake by the body.

Full Information

First Posted
December 28, 2021
Last Updated
March 6, 2023
Sponsor
Hvidovre University Hospital
Collaborators
Institute of Biomedical Sciences, SUND, University of Copenhagen
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1. Study Identification

Unique Protocol Identification Number
NCT05189353
Brief Title
The Importance of Ghrelin for Glucose Metabolism After Sleeve Gastrectomy
Official Title
The Importance of Ghrelin for Glucose Metabolism After Sleeve Gastrectomy
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Recruiting
Study Start Date
January 14, 2022 (Actual)
Primary Completion Date
June 2023 (Anticipated)
Study Completion Date
June 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hvidovre University Hospital
Collaborators
Institute of Biomedical Sciences, SUND, University of Copenhagen

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 overall aim is to delineate the contribution of ghrelin to glucose tolerance after sleeve gastrectomy. The hypothesis is that decreased concentration of ghrelin after SG is of importance for improved insulin secretion and glucose tolerance seen after SG. The expectation is therefore that infusion of ghrelin will impair insulin secretion and glucose tolerance compared with a control day without ghrelin infusion.
Detailed Description
Roux-en-Y gastric bypass (RYGB) and sleeve gastrectomy (SG) are bariatric procedures. Overwhelming evidence support bariatric surgery as the most effective treatment for severe obesity and related metabolic comorbidities, particularly type 2 diabetes mellitus. The mechanisms of improved glycaemic control after SG are not fully understood and differ from those of RYGB. Interestingly, there is demonstrated a markedly lower secretion of the orexigenic hormone ghrelin after SG compared with both RYGB and unoperated obese controls. Hence, the decreased level of ghrelin could be of major importance in relation to the improved glucose tolerance after SG. Ghrelin is secreted from the gastric mucosa in the fasting state and decreases in response to food intake. Administration of exogenous ghrelin reduces insulin sensitivity and glucose tolerance in healthy humans and contributes to hyperglycaemia. In accordance, ghrelin receptor knockout in mice improves glucose sensitivity and enhances glucose-stimulated insulin secretion. On this background the investigators hypothesize that the markedly reduced secretion of ghrelin after SG could therefore be of particularly importance for the improved glucose tolerance after this procedure. This present study is complementary to an on-going study in SG operated subjects, where the role of ghrelin for appetite and insulin secretion during a mixed meal followed by an ad libitum meal are investigated. In the present study the effect of ghrelin on insulin secretion and insulin sensitivity is thoroughly investigated using methods eliminating the effect of other hormones on glucose metabolism. Ghrelin will be infused in physiological doses aiming for plasma concentration after SG resembling the pre-operative plasma concentrations. Specific aim is to evaluate the effect of ghrelin on both alpha and beta cell function as well as on liver and peripheral insulin sensitivity in individuals with SG using matched controls. The subjects will be investigated with both glucose and glycerol tracers, IVGTT and a hyperinsulinemic euglycaemic clamp.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bariatric Surgery Candidate, Glucose Metabolism Disorders
Keywords
Ghrelin, Gastric sleeve, Glucose metabolism

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Masking Description
Single randomized clinical trial
Allocation
Randomized
Enrollment
24 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Gastric sleeve operated
Arm Type
Experimental
Arm Description
12 subjects with normal glucose tolerance (NGT) operated with SG minimum 12 month earlier
Arm Title
Matched control group
Arm Type
Placebo Comparator
Arm Description
12 weight-matched unoperated subjects with NGT
Intervention Type
Other
Intervention Name(s)
Ghrelin
Intervention Description
Ghrelin infusion
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
Saline infusion
Primary Outcome Measure Information:
Title
The difference in disposition index between the two study days with and without ghrelin in fusion in the SG operated group
Description
The first phase insulin response will be related to the ambient insulin sensitivity by calculating the disposition index (FPIR x M-value).
Time Frame
0-180 minutes
Secondary Outcome Measure Information:
Title
The difference in first phase insulin response (FPIR) between the two study days with and without ghrelin in fusion in the SG operated group
Description
Estimation of beta-cell function, calculated from insulin secretion rate using c-peptid and deconvolution from 0-10 min.
Time Frame
0-10 minutes (IVGTT)
Title
The difference in Insulin sensitivity (M-value) between the two study days with and without ghrelin in fusion in the SG operated group
Description
When a steady state is reached at the end of the clamp, the glucose infusion rate represents insulin-mediated glucose uptake by the body.
Time Frame
160-180 minutes (the end of the clamp)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Sleeve gastrectomy-operated > 12 months prior to inclusion Weight stable (+/- 3 kg during the last 3 months) Fasting glucose < 7,0 mmol/l / HbA1c < 48 mmol/mol pre- and postoperative Signed written informed consent Exclusion Criteria: Pregnancy or breastfeeding. Haemoglobin < 6,5 mM.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Marie-Louise Dichman, MD
Phone
+4526710371
Email
marie-louise.dichman@regionh.dk
First Name & Middle Initial & Last Name or Official Title & Degree
Nora Hedbäck, MD
Phone
38620340
Email
nora.elisabeth.hedbaeck.01@regionh.dk
Facility Information:
Facility Name
Hvidovre Universitets Hospital
City
Hvidovre
ZIP/Postal Code
2650
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marie-Louise Dichman

12. IPD Sharing Statement

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The Importance of Ghrelin for Glucose Metabolism After Sleeve Gastrectomy

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