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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT02331420
Other study ID # 4569/14
Secondary ID
Status Not yet recruiting
Phase N/A
First received January 2, 2015
Last updated January 5, 2015
Start date February 2015
Est. completion date July 2017

Study information

Verified date January 2015
Source Catholic University of the Sacred Heart
Contact n/a
Is FDA regulated No
Health authority Italy: Ethics Committee
Study type Interventional

Clinical Trial Summary

To assess the impact of weight loss due to bariatric surgery, as compared to the effect of optimal medical therapy alone on endothelial function, subclinical atherosclerosis, cardiovascular autonomic function in obese patient affected by type 2 diabetes.The study consists in a 2-arm randomized trial, in which patients will be randomly assigned to bariatric surgery or optimal medical therapy. Each patient will be studied at baseline (T0) and 12 months thereafter (T1).


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 58
Est. completion date July 2017
Est. primary completion date January 2017
Accepts healthy volunteers No
Gender Both
Age group 40 Years to 70 Years
Eligibility Inclusion Criteria:

- type 2 diabetes: the American Diabetes Association (ADA) recommends the following criteria for diagnosis of diabetes: HbA1c =6.5% OR fasting plasma glucoseā€” =126 mg/dL (7.0 mmol/L) OR 2-hour plasma glucose =200 mg/dL (11.1 mmol/L) during an oral glucose tolerance test; 75-g glucose load should be used OR random plasma glucose concentration =200 mg/dL (11.1 mmol/L) in persons with symptoms of hyperglycemia or hyperglycemic crisis;

- indication to bariatric surgery: BMI =35 kg/m2 and one or more obesity related co-morbidities, including Type 2 Diabetes Mellitus.

Exclusion Criteria:

- overt cardiovascular disease (as assessed by clinical evaluation, physical examination, 12-lead ECG, 2D-echocardiogram);

- smoking habit;

- associated medical conditions, as chronic kidney disease (defined as creatinine clearance <60 mL/min/L.73m2), liver cirrhosis, malignancies, chronic congestive heart failure, acute or chronic inflammatory disease;

- specific contraindication to bariatric surgery;

- pregnancy;

- medical conditions requiring acute hospitalization;

- psychological conditions which may hamper patient's cooperation;

- geographic inaccessibility.

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Diagnostic


Related Conditions & MeSH terms


Intervention

Procedure:
Gastric bypass
A subcardial gastric pouch with a 30±10 ml capacity will be created by sectioning the stomach with a linear stapler 3-4 cm horizontally on the lesser curve, 4 cm distal to the e-g junction, and then vertically until attainment of the angle of Hiss. After identification of the Treitz ligament, the jejunum will be transected at 100 cm from the ligament of Treitz and the two stumps will be closed. The distal stump will be anastomosed to the distal end of the gastric pouch. The preferred gastro-jejunal anastomosis is the totally hand-sewn one, but it can be performed using any other the technique the surgeon is more familiar with. Finally, the proximal stump of the transacted bowel will be joined end-to-side to the jejunum 150 cm distal to the gastro-enterostomy.
Behavioral:
Medical therapy
Assessment and treatment by a multidisciplinary team (diabetologist, dietitian, nurse); Planned visits at baseline and at 1, 3, 6, 9, 12, and 24 months after study entry; Oral hypoglycemic agents and insulin doses optimized on an individual basis with the aim of reaching a glycated hemoglobin level of less than 7%; Programs for diet and lifestyle modification, including reduced overall energy and fat intake (<30% total fat, <10% saturated fat, and high fiber content) and increased physical exercise (=30 minutes of brisk walking every day, possibly associated with moderate-intensity aerobic activity twice a week); low-calorie diet (every day: 50% carbohydrate, 30% protein and 20% lipids).

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Catholic University of the Sacred Heart

Outcome

Type Measure Description Time frame Safety issue
Primary Subclinical Atherosclerosis (ecographic assessment of carotid artery intima-media thickness) ecographic assessment of carotid artery intima-media thickness 12 months No
Primary Endothelial Function (ecographic assessment of flow-mediated dilation and nitrate mediated dilation) ecographic assessment of flow-mediated dilation and nitrate mediated dilation 12 months No
Primary Cardiac autonomic function (heart rate variability measurements on 24-hour Holter ECG recordings) heart rate variability measurements on 24-hour Holter ECG recordings 12 months No
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