Weight-loss and Gut-brain Interactions
Obesity

About this trial
This is an interventional treatment trial for Obesity
Eligibility Criteria
Inclusion Criteria: In order to be eligible to participate in this study, a subject must qualify for weight loss surgery with LAGB or RYGB, as evaluated by a physician at intake for surgery. Furthermore, subjects must meet all of the following criteria:
- Subject, male or female, is age 18 to 60 years of age.
- Subject must be able to understand and be willing to sign an informed consent document.
- Subject must be willing and able to participate in all aspects of the study and agree to comply with all study requirements for the duration of the study.
- Subject has a body mass index (BMI) of 40 - 45 or 35 to 39.9 plus one or more co-morbid diseases expected to improve with weight loss, including but not limited to hypertension, dyslipidemia, obstructive sleep apnea, or diabetes mellitus.
- Subject must be of sufficient and stable medical health, as evaluated by physician at intake.
- Subject must have failed standard obesity therapy of diet, exercise, behaviour modification, and pharmacologic agents either alone or in combination, as assessed at the intake for surgery by a physician.
- For the fMRI measurements inclusion criteria are as follows: not having any metallic fragments in the body, being right-handed. Because of the different brain laterality in left- and right-handed subjects we chose to include only right-handed subjects. Hence the results can be compared between the subjects.
Exclusion Criteria:
- - Subject has history of/or signs and/or symptoms of gastro-duodenal ulcer disease, as evaluated by physician at intake for the surgery.
- Subject has had significant weight loss in the last 3 months (>5kg).
- Subject has a history or is diagnosed with eating disorders.
- Subject has renal and/or hepatic insufficiency, as evaluated by physician at intake.
- Subject has thyroid disease, which is not controlled with medication, as evaluated by physician at intake for the surgery.
- Female subject who is pregnant (i.e., has a positive urine or blood pregnancy test prior to the procedure), is suspected to be pregnant, is lactating or is of childbearing potential but refuses to use adequate contraception during the study.
- Female subject who started birth control pills less than 3 months before enrollment, or who plans to start taking birth control pills during the study.
- Subjects who cannot discontinue either prescription or over the counter weight loss medications for at least 30 days prior to the start of the study as well as during the trial period.
- Subjects who have started medications within the last 3 months that are known to cause weight gain.
- Subjects who have cardiac pacemakers or other electronic implantable devices.
- Subjects who have psychiatric disease including but not limited to manic-depressive disorder, schizophrenia, borderline personality disorder, depression or suicidal tendencies.
- Subject currently uses or has a history of illicit drug(s) or abuses alcohol (defined as regular or daily consumption of more than 4 alcoholic drinks per day).
- Subject has participated in a clinical study with an investigational new drug, biological, or therapeutic device within ≤ 28 days prior to enrollment in this study, and does not agree to abstain from participation in other clinical trials of any kind during this study.
- Presence of contra-indications for f-MRI, as mentioned in the screening form and informed consent of the faculty of psychology (see section E2 and F1).
- Claustrophobia
- Being left-handed
- Metallic fragments in the body
Sites / Locations
- Maastricht University (metabolic research unit Maastricht (MRUM))
Arms of the Study
Arm 1
Arm 2
Arm 3
Active Comparator
Active Comparator
Active Comparator
Roux- and Y bypas surgery (RYGB)
Laparoscopic adjustable gastric banding (LAGB)
Very Low Calorie Diet (VLCD)
One subject group will lose 10% of initial body weight using RYGB. RYGB is an operation that first divides the stomach into a small upper pouch and a much larger lower "remnant" pouch and then re-arranges the small intestine to connect to both, in this way bypassing part of the small intestine.
One subject group will lose 10% of initial body weight using LAGB. With LAGB an inflatable band is placed around the upper part of the stomach to create a smaller stomach pouch. This slows and limits the amount of food that can be consumed at one time giving the opportunity for the sense of satiety to be met. It does not decrease gastric emptying time.
One subject group will lose 10% of initial body weight using a VLCD. There are no risks for the subjects in consuming the VLCD (Modifast, together with the recommended fruit and vegetables) as the macronutrient composition and vitamins/minerals content meet the Dutch recommended daily allowance.