NCT02944500Active, not recruitingPhase 4
Saxenda: Underlying Mechanisms and Clinical Outcomes
Source: ClinicalTrials.gov · Last updated 1 May 2026
Brief summary (registry, in English)
The purpose of this protocol is to investigate the effect of treatment with the study drug Liraglutide, a GLP-1 receptor agonist, on centers of the brain that control appetite and food intake.
- Status (registry)
- Active, not recruiting
- Phase (registry)
- Phase 4
- Study type
- Interventional
- Enrollment
- 28 (actual)
- First submitted
- 24 Oct 2016
- Start date
- Nov 2016
- Primary completion date
- Jun 2027
- Lead sponsor
- Beth Israel Deaconess Medical Center
- Diseases
- Obesity
- NCT number
- NCT02944500
What you commit to
- Study type: Interventional · Phase 4
- Participants enrolled: 28
- From Nov 2016 to the primary completion date, Jun 2027
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Any change in the dosage of hormonal contraceptive medications (birth control pills, implanon). Subjects should remain on same medication/ same dose during the time of the entire study.
- Subjects taking the following medications: warfarin, steroids (inhaled or systemic due to reduced hypoglycemic effect), and subjects on other hormones (LHRH analogs etc).
- Subjects with any type of bioimplant activated by mechanical, electronic, or magnetic means (e.g. cochlear implants, pacemakers, neuron or biostimulators, electronic infusion pumps, etc.)
- Subjects with any type of metallic implant that could potentially be displaced or damaged during MRI, such as aneurysm clips, metallic skull plates, surgical implants etc. or metal containing tattoos
- Weight loss surgery or gastrectomy
Other illness
- Moderate, or severe hepatic impairment
- Hypersensitivity to the active substance or any of the excipients in liraglutide
- History of diabetic ketoacidosis
- Congestive heart failure
- Inflammatory conditions like inflammatory bowel disease, Rheumatoid arthritis etc
- Untreated thyroid disease like hypothyroidism or hyperthyroidism
- Personal or family history of MEN II or medullary thyroid cancer
- Uncontrolled cardiac impairment, circulatory impairment, or inability to perspire (poor thermoregulatory function)
- Significant sensory or motor impairment
- Epilepsy, particularly photo-sensitive epilepsy, which may place the individual at a higher risk for adverse events during fMRI scanning with visual stimulation
- Uncontrolled infectious diseases (e.g. HIV, hepatitis, chronic infections etc)
- Any uncontrolled endocrine condition, e.g Cushing's, Acromegaly, etc
- Any cancers or lymphoma
- Eating disorders like anorexia, bulimia
- Any changes in medications that affect brain function, e.g. anti-depressants, anti-psychotics, anti-anxiety, anti-seizure medications, antihypertensives etc (subjects should remain on same medication/ same dose during the time of the entire study).
Lab values
- Moderate (creatinine clearance of 30-59 ml/min) and severe renal impairment (creatinine clearance below 30 ml/min) and end-stage renal disease
- Severe hypertriglyceridemia (triglycerides \>500 mg/dl)
Other
- Women who are breastfeeding, pregnant, or wanting to become pregnant.
- Women using metal IUD
- EKG abnormalities (as listed above)
- Gastroparesis
- Pancreatitis
- Gallstones- as they may cause increased risk of pancreatitis
- Alcohol consumption- the maximum quantity for men is 140g-210g per week. For women, the range is 84g-140g per week or drinking as consuming no more than two drinks a day for men and one for women. Alcohol can cause increased risk of pancreatitis and hypoglycemia.
- Subjects on any oral anti-diabetic agent except metformin
- Anxiety of small spaces and/or claustrophobia
- Subjects with neurological or psychological problems which may interfere with or complicate testing (e.g. presence of titubation)
- Body weight above the limitation of the MRI scanning table (330lbs/150 Kg) or body dimensions that could difficult the performance of the scan.
- Subjects who cannot adhere to the experimental protocol for any reason
- Anemia with Hgb less than 10
- Vegetarians- as food images presented will include numerous non-vegetarian items and thus will not be appealing as high calorie food items.
- Suicidality, as measured by the MSSI at screening visit.
Who the study is looking for
- Obese: BMI\> 30 kg/m2 or \>27 kg/m2 with comorbidities (including but not limited to insulin resistance, hypertension, dyslipidemia, cardiovascular disease, stroke, sleep apnea, gallbladder disease, hyperuricemia and gout, and osteoarthritis).
Age in the registry: 18 years to 100 years · Sex: All · Accepts healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Beth Israel Deaconess Medical Center General Clinical Research Center Coordinator of this site? Confirm its status | Boston | United States | Unknown status |
Related publications
This page is information, not medical advice. Discuss any trial with your doctor.