Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Texas Tech University
With
Novo Nordisk A/S
Age
18–60
Sex
ALL
Healthy volunteers
Accepted
You may be eligible if
Age 18-60 years
BMI 30-50 kg/m2
You may not be if
Participants unable or unwilling to provide informed consent.
Participants with motor, visual or hearing impairment.
Females with irregular menstrual cycles (onset of menstruation greater than 1 week from expected data during the last 3 months).
Females who are currently breastfeeding or intend to start breastfeeding.
Participants with diagnosed diabetes mellitus (type 1 or type 2) or uncontrolled hypertension, history of ischemic heart disease, stroke, neurological disease.
Participants with current severe psychiatric illnesses (e.g. psychosis, schizophrenia, bipolar disorders, depression).
Participants experiencing current suicidal ideation, and recent or past suicide attempts.
Participants with history of psychiatric hospitalization.
Participants who are currently on (or have been on within the past 4 weeks) any medication in the broader drug classes of anti-depressant, anti-epileptic, or anti-anxiety medicines will be excluded (as these affect fMRI-FCR in the brain).
Participants with contraindications for MRI scanning.
1. aneurism clips
2. any implanted medical devices (pacemaker, neurostimulator)
3. known pregnancy
4. shrapnel in body or any injury to eye involving metal
5. any ferrous metal in body
Participants with a history of diagnosed eating disorders such as bulimia nervosa, anorexia nervosa and severe binge eating disorder.
Participants with a history of diagnosed substance abuse or alcohol abuse.
Patients experiencing persistent loss of appetite, nausea or vomiting within the last 4 weeks without known cause (e.g. flu, food poisoning).
Participants who have been involved in a weight loss intervention program (including anti-obesity medication) within the past 3 months (and or loss \>10% of body weight) or who have ever had bariatric surgery or have weight loss devices implanted.
Current smokers (smoked within the last 30 days).
The receipt of any investigational drug within (3 months) prior to this trial.
Previous participation in this trial (i.e. randomized).
Unable or unwilling to consume required study meals for any reason (e.g. dietary restrictions, allergies, or aversions to any of the food items used in the study).
Contraindications to study medications,
* Subject with a personal or family history of medullary thyroid carcinoma (MTC).
* Subject with multiple endocrine neoplasia syndrome 2 (MEN 2).
* Allergic to Liraglutide or any of the ingredients in Saxenda® (i.e. Active ingredient: liraglutide; Inactive ingredients: disodium phosphate dehydrate, propylene glycol, phenol and water for injection)
* Women who are pregnant, or have the intention of becoming pregnant.
Taking other GLP-1 receptor agonists (currently or in the past 3 months).
Current severe problems with stomach, such as slowed emptying of the stomach (gastroparesis) or problems with digesting food.
Current or past known serious chronic illness of liver, kidney and pancreas.
Current or recent (30 days) depression or suicidal thoughts.
Current fasting plasma glucose 126mg/dL or higher or HbA1c 6.5% or higher, or alanine aminotransferase (ALT), aspartate aminotransferase (AST), creatinine, blood urea nitrogen (BUN) 10% above normal range for the assay.
Clareo Health | To Predict Weight Loss Response to Liraglutide (Saxenda®), From fMRI-based Determination of Food Cue Reactivity
