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SLEEVEDIAB To Explore the Early and Late Metabolic Effects of Sleeve Gastrectomy in Obese Patients (SLEEVEDIAB)

Primary Purpose

Severe Obesity, Type 2 Diabetes

Status
Unknown status
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Caloric restriction
No caloric restriction
Sponsored by
University Hospital, Montpellier
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Severe Obesity focused on measuring Type 2 diabetes, Obesity, Sleeve gastrectomy, Insulin, GLP-1

Eligibility Criteria

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

Inclusion Criteria:

  • written informed consent
  • Age between 18-65 years (inclusive)
  • Men or women receiving effective contraception, postmenopausal or sterile
  • type 2 diabetes treated with no drugs or oral anti-diabetic agents metformin, sulfonylurea or glinides
  • Body mass index 35 kg / m² or above
  • eligible to bariatric surgery according to HAS criteria

Exclusion Criteria:

  • Treatment of diabetes with GLP1 analogues, DPP-IV (dipeptidyl-peptidase IV) or insulin
  • Treatment with drugs that modify glucose homeostasis: glucocorticoids, anorexigens, antihistaminics, psychotropic drugs especially serotonergic antidepressants (except for the occasional use of a hypnotic or anxiolytic), atropine, laxatives, thyroid hormones (with the exception of a substitution dose ensuring a stable euthyroid at baseline), beta blockers, diuretics
  • Pregnancy, intention of being pregnant, breastfeeding.
  • Inability to understand the nature and aims of the study or to communicate with the investigator- High probability of non
  • compliance with the protocol
  • Simultaneous participation in another trial
  • No affiliation to the French social security
  • Loss of personal capacity resulting in state protection
  • Deprivation of liberty by judicial or administrative decision

Sites / Locations

  • CHU MontpellierRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Arm with caloric restriction

Arm without caloric restriction

Arm Description

Patients in this arm will have, during 7 days before surgery, a caloric restriction of 1000 kcal per day compared to the usual food intake. They will be hospitalized during this period. Intervention: caloric restriction

Patients in this arm will not have a caloric restriction before surgery. Intervention: No caloric restriction

Outcomes

Primary Outcome Measures

Change of area under the curve of post prandial glycemia

Secondary Outcome Measures

Change in insulin sensitivity, Change in insulin secretion, Change in incretins

Full Information

First Posted
December 17, 2013
Last Updated
December 2, 2014
Sponsor
University Hospital, Montpellier
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1. Study Identification

Unique Protocol Identification Number
NCT02076880
Brief Title
SLEEVEDIAB To Explore the Early and Late Metabolic Effects of Sleeve Gastrectomy in Obese Patients
Acronym
SLEEVEDIAB
Official Title
Investigation of Endocrin-metabolic Modifications Related to Diabetes Improvement After Sleeve Gastrectomy in Severly Obese
Study Type
Interventional

2. Study Status

Record Verification Date
September 2013
Overall Recruitment Status
Unknown status
Study Start Date
November 2013 (undefined)
Primary Completion Date
November 2016 (Anticipated)
Study Completion Date
November 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Montpellier

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Sleeve gastrectomy is a restrictive procedure based on the removal of a large part of the gastric fundus. According to a recent randomized study, weight loss and resolution of diabetes are comparable to that obtained after gastric by-pass (79.7 % versus 80.3%), but with a lower morbidity. The mechanisms involved in the rapid resolution of diabetes after sleeve gastrectomy remain poorly understood, as no specific study in patients with type 2 diabetic obese are available. An increase in post- absorptive levels of Glucagon-like Peptide 1(GLP-1), Peptide YY(PYY) and insulin has been reported, but in non-diabetic subjects mostly. The important caloric restriction in the early postoperative period indeed improves hepatic insulin resistance, regardless of weight loss. Specific metabolic and hormonal effects of this surgical procedure cannot be excluded.The aim of our study is to explore the early and late metabolic effects of sleeve gastrectomy in severely obese patients with non-insulin-treated type 2 diabetes. We will also evaluate insulin sensitivity, insulin secretion and incretin effect. We will include 14 obese patients with type 2 diabetes, considered eligible to bariatric surgery according to HAS criteria, and whose diabetes treatment involves only metformin, sulfonylurea and glinides. They will be randomized to a 1-week caloric restriction period or no caloric restriction, immediately before surgery. Test meals with dosages of blood glucose, insulin, C-peptide, adiponectin, leptin, GLP-1, PYY and ghrelin will be performed before and after caloric restriction, and 1 week, 3 month, 6 month and 12 month after surgery.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Severe Obesity, Type 2 Diabetes
Keywords
Type 2 diabetes, Obesity, Sleeve gastrectomy, Insulin, GLP-1

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Arm with caloric restriction
Arm Type
Experimental
Arm Description
Patients in this arm will have, during 7 days before surgery, a caloric restriction of 1000 kcal per day compared to the usual food intake. They will be hospitalized during this period. Intervention: caloric restriction
Arm Title
Arm without caloric restriction
Arm Type
Experimental
Arm Description
Patients in this arm will not have a caloric restriction before surgery. Intervention: No caloric restriction
Intervention Type
Other
Intervention Name(s)
Caloric restriction
Intervention Description
Caloric restriction of 1000 kcal per day compared to the usual food intake. usual breakfast of the patient (possibly limited in quantity) midday and evening meals from mixed and dehydrated meals, soups with protein and dairy desserts sweetened
Intervention Type
Other
Intervention Name(s)
No caloric restriction
Intervention Description
No change in eating habits to patients in this arm
Primary Outcome Measure Information:
Title
Change of area under the curve of post prandial glycemia
Time Frame
Baseline to day 7 after surgery
Secondary Outcome Measure Information:
Title
Change in insulin sensitivity, Change in insulin secretion, Change in incretins
Time Frame
Blood samples at D-15, D-7 before surgery, D7, D80, D170, D350 after surgery

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: written informed consent Age between 18-65 years (inclusive) Men or women receiving effective contraception, postmenopausal or sterile type 2 diabetes treated with no drugs or oral anti-diabetic agents metformin, sulfonylurea or glinides Body mass index 35 kg / m² or above eligible to bariatric surgery according to HAS criteria Exclusion Criteria: Treatment of diabetes with GLP1 analogues, DPP-IV (dipeptidyl-peptidase IV) or insulin Treatment with drugs that modify glucose homeostasis: glucocorticoids, anorexigens, antihistaminics, psychotropic drugs especially serotonergic antidepressants (except for the occasional use of a hypnotic or anxiolytic), atropine, laxatives, thyroid hormones (with the exception of a substitution dose ensuring a stable euthyroid at baseline), beta blockers, diuretics Pregnancy, intention of being pregnant, breastfeeding. Inability to understand the nature and aims of the study or to communicate with the investigator- High probability of non compliance with the protocol Simultaneous participation in another trial No affiliation to the French social security Loss of personal capacity resulting in state protection Deprivation of liberty by judicial or administrative decision
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Florence GALTIER, MD
Email
f-galtier@chu-montpellier.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Eric RENARD, PU-PH
Email
e-renard@chu-montpellier.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Florence GALTIER, MD
Organizational Affiliation
Montpellier University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
CHU Montpellier
City
Montpellier
ZIP/Postal Code
34295
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
GALTIER Florence
Email
f-galtier@chu-montpellier.fr
First Name & Middle Initial & Last Name & Degree
GALTIER Florence, MD

12. IPD Sharing Statement

Learn more about this trial

SLEEVEDIAB To Explore the Early and Late Metabolic Effects of Sleeve Gastrectomy in Obese Patients

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