Early Changes of Diabetes Parameters After Obesity Therapy (ECODO)
Primary Purpose
Bariatric Surgery Candidate
Status
Unknown status
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
Laparoscopic sleeve gastrectomy
Laparoscopic Roux-en-Y gastric bypass
Caloric restriction diet
easy digestible diet
Sponsored by

About this trial
This is an interventional treatment trial for Bariatric Surgery Candidate
Eligibility Criteria
Inclusion Criteria:
- BMI (Body Mass Index) ≥ 35 kg/m2
- Clinical diagnosis of type II diabetes or impaired glucose metabolism (Prediabetes: HbA1c > 5,7%, fasting glucose in capillary blood > 110 mg/dl - diagnosed by blood glucose test at the first study examination)
- Regarding the patients of the surgical groups: Indication to surgical therapy of obesity (laparoscopic sleeve gastrectomy or Roux-en-Y gastric bypass). The indication to surgery is independent of the study. The surgeon decides about that in the clinical routine according to the German S3 guideline.
- Written consent to participate int he study
Exclusion Criteria:
- Medication use which affects glucose metabolism, except for diabetes medication (for example: glucocorticoids)
- Insulin need >1,0 IU/kg/d
- Experimental diabetes medication within the last three months
- Pregnancy
- Gastrointestinal diseases
- Uncontrolled hypo- or hyperthyroidism
- Status after bariatric or other gastrointestinal surgery
Sites / Locations
- University of HohenheimRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Experimental
Other
Arm Label
LSG group
LRYGB group
Control group
Arm Description
Laparoscopic sleeve gastrectomy
Laparoscopic Roux-en-Y gastric bypass
Caloric restriction
Outcomes
Primary Outcome Measures
Change of insulin
Blood insulin is measured during a Mixed Meal Tolerance Test (MMTT). It is used to calculate the Homeostasis Model Assessment (HOMA) and Matsuda Insulin Sensitivity Index
Change of blood glucose
Blood glucose is measured during a Mixed Meal Tolerance Test (MMTT). It is used to calculate the Homeostasis Model Assessment (HOMA) and Matsuda Insulin Sensitivity Index
Secondary Outcome Measures
Full Information
NCT ID
NCT02553213
First Posted
September 4, 2015
Last Updated
May 14, 2018
Sponsor
University of Hohenheim
Collaborators
University Hospital Tuebingen, Karl-Olga-Krankenhaus Stuttgart
1. Study Identification
Unique Protocol Identification Number
NCT02553213
Brief Title
Early Changes of Diabetes Parameters After Obesity Therapy
Acronym
ECODO
Official Title
Early Changes of Diabetes Parameters After Obesity Therapy
Study Type
Interventional
2. Study Status
Record Verification Date
May 2018
Overall Recruitment Status
Unknown status
Study Start Date
July 2015 (undefined)
Primary Completion Date
May 2019 (Anticipated)
Study Completion Date
July 2019 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Hohenheim
Collaborators
University Hospital Tuebingen, Karl-Olga-Krankenhaus Stuttgart
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The aim of the study is to investigate, if bariatric surgery or the related caloric restriction causes the significant improvement of glucose metabolism, which has been found in bariatric patients.
Detailed Description
Previous studies have shown, that laparoscopic Roux-en-Y gastric bypass (LRYGB), and also laparoscopic sleeve gastrectomy (LSG) leed to a significant improvement of glucose metabolism and in many cases to a complete remission of diabetes type II in obese patients. It is still unclear which mechanisms underlie these changes. Since the positive effects of bariatric surgery have been investigated within few days after surgical intervention, before significant weight loss has been achieved, the caloric restriction has been discussed as a possible mechanism.
The aim of the study is to investigate, if bariatric surgery or the related caloric restriction causes the significant improvement of glucose metabolism, which has been found in bariatric patients. Therefore, the investigator will examine obese patients with diabetes type II or impaired glucose metabolism regarding possible metabolic changes within few days after bariatric surgery (LSG or LRYGB) or caloric restriction only.
Group I: Patients undergoing LSG; Group II: Patients undergoing LRYGB; Group III (Control group): Patients undergoing caloric restriction;
Dietetic, anthropometric, metabolic and hormonal parameters will be measured. Primary outcome marker is the insulin sensitivity according to Matsuda (MISI).
The project is a prospective, controlled study. Study examinations will be performed before intervention, and one, two, three, four and five days after (start of) intervention, as well after one month.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bariatric Surgery Candidate
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
30 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
LSG group
Arm Type
Experimental
Arm Description
Laparoscopic sleeve gastrectomy
Arm Title
LRYGB group
Arm Type
Experimental
Arm Description
Laparoscopic Roux-en-Y gastric bypass
Arm Title
Control group
Arm Type
Other
Arm Description
Caloric restriction
Intervention Type
Other
Intervention Name(s)
Laparoscopic sleeve gastrectomy
Intervention Description
The surgical procedure and aftercare is indicated and performed according to the routine clinical setting of the Hospital. Patients stay 5 days stationary after surgical treatment. They receive a defined easy digestible diet, starting with liquid and mash food.
Intervention Type
Other
Intervention Name(s)
Laparoscopic Roux-en-Y gastric bypass
Intervention Description
The surgical procedure and aftercare is indicated and performed according to the routine clinical setting of the Hospital. Patients stay 5 days stationary after surgical treatment. They receive a defined easy digestible diet, starting with liquid and mash food.
Intervention Type
Other
Intervention Name(s)
Caloric restriction diet
Intervention Description
Patients of the control group do not undergo surgical treatment. They undergo a caloric restriction diet for 5 days. This diet is adapted to the postoperative diet of the patients included in the two other groups.
Intervention Type
Other
Intervention Name(s)
easy digestible diet
Primary Outcome Measure Information:
Title
Change of insulin
Description
Blood insulin is measured during a Mixed Meal Tolerance Test (MMTT). It is used to calculate the Homeostasis Model Assessment (HOMA) and Matsuda Insulin Sensitivity Index
Time Frame
Within 5 days after surgery or 5 days after start of caloric restriction
Title
Change of blood glucose
Description
Blood glucose is measured during a Mixed Meal Tolerance Test (MMTT). It is used to calculate the Homeostasis Model Assessment (HOMA) and Matsuda Insulin Sensitivity Index
Time Frame
Within 5 days after surgery or 5 days after start of caloric restriction
Other Pre-specified Outcome Measures:
Title
Changes regarding markers of glucose metabolism
Description
HbA1c, C-Peptid, insulin and fasting glucose
Time Frame
Within 5 days after surgery or 5 days after start of caloric restriction
Title
Changes of body weight
Time Frame
Within 5 days after surgery or 5 days after start of caloric restriction
Title
Changes of blood lipids
Description
High density lipoprotein, low density lipoprotein, triglycerides, free fatty acids
Time Frame
Within 5 days after surgery or 5 days after start of caloric restriction
Title
Changes concerning the intake of calories and nutrients
Description
Measured by using nutritional protocols
Time Frame
Within 5 days after surgery or 5 days after start of caloric restriction
Title
Changes of gastrointestinal hormones
Description
Glucagon-like peptide-1, Ghrelin, Glucose-dependent insulinotropic peptide
Time Frame
Within 5 days after surgery or 5 days after start of caloric restriction
Title
Changes of adiponectin
Time Frame
Within 5 days after surgery or 5 days after start of caloric restriction
Title
Changes of bile acids
Time Frame
Within 5 days after surgery or 5 days after start of caloric restriction
Title
Changes of gut microbiota composition
Time Frame
Within 5 days after surgery or 5 days after start of caloric restriction
Title
Changes of body height
Time Frame
Within 5 days after surgery or 5 days after start of caloric restriction
Title
Changes of body composition
Description
measured by Body Impedance Analysis
Time Frame
Within 5 days after surgery or 5 days after start of caloric restriction
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:
BMI (Body Mass Index) ≥ 35 kg/m2
Clinical diagnosis of type II diabetes or impaired glucose metabolism (Prediabetes: HbA1c > 5,7%, fasting glucose in capillary blood > 110 mg/dl - diagnosed by blood glucose test at the first study examination)
Regarding the patients of the surgical groups: Indication to surgical therapy of obesity (laparoscopic sleeve gastrectomy or Roux-en-Y gastric bypass). The indication to surgery is independent of the study. The surgeon decides about that in the clinical routine according to the German S3 guideline.
Written consent to participate int he study
Exclusion Criteria:
Medication use which affects glucose metabolism, except for diabetes medication (for example: glucocorticoids)
Insulin need >1,0 IU/kg/d
Experimental diabetes medication within the last three months
Pregnancy
Gastrointestinal diseases
Uncontrolled hypo- or hyperthyroidism
Status after bariatric or other gastrointestinal surgery
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Anna Schweinlin
Phone
+4971145924880
Email
anna.schweinlin@uni-hohenheim.de
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Stephan C. Bischoff, Prof.
Organizational Affiliation
Department of Nutritional Medicine, University of Hohenheim, Stuttgart, Germany
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Alfred Königsrainer, Prof.
Organizational Affiliation
Department of General, Visceral, and Transplant Surgery, University Hospital Tübingen, Germany
Official's Role
Study Director
Facility Information:
Facility Name
University of Hohenheim
City
Stuttgart
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Anna Schweinlin
Phone
+4971145924880+4970712986584
Email
anna.schweinlin@uni-hohenheim.de
12. IPD Sharing Statement
Learn more about this trial
Early Changes of Diabetes Parameters After Obesity Therapy
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