Obesity
Conditions
Brief summary
Title: Embolization of Gastric Arterial Supply for Weight Loss Sample size: 10 patients Study Population: Morbidly obese patients who were seen by the bariatric surgery program at Toronto Western Hospital but are either not interested or not eligible for surgery. Study Design: Single center, randomized, prospective, non-blinded pilot study. Study Duration: 12 months (November 2015 - December 2015). Agent: 150-250 micron polyvinyl alcohol particles Primary objective: To further evaluate the safety of embolization of the left gastric and gastroepiploic arteries. To determine if either or both will result in significant weight loss and decrease in waist circumference among obese patients. Primary objective measure: The number of adverse events in a 1 year period will be recorded. The weight change from baseline will be recorded.
Interventions
PROCEDUREEmbolization of Left Gastric Artery
Left gastric artery will be embolized to stasis with 150-250 micron polyvinyl alcohol particles
PROCEDUREEmbolization of Gastroepiploic Artery
Gastroepiploic artery will be embolized to stasis with 150-250 micron polyvinyl alcohol particles
Sponsors
University Health Network, Toronto
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)
Eligibility
Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No
Inclusion criteria
* Meet standard eligibility criteria for bariatric surgery. BMI of \>= 40 -or- BMI of \>=35 with one of the following comorbid conditions: hypertension, type 2 diabetes, obstructive sleep apnea, coronary artery disease
Exclusion criteria
Basic Unable to provide informed consent (legally authorized representative is acceptable) Unable or unwilling to come for follow up appointments Age \< 18 or \>80 Weight \>400 lbs or 180kg due to weight limits on angiographic tables Moderate or severe allergy to iodinated contrast media not amenable to premedication as defined by the ACR contrast guidelines Pregnant, breastfeeding or actively trying to become pregnant in the next year Inability to lie flat for the duration of the procedure Limited life expectancy \< 1 year Patient enrolled in another interventional study, they will be permitted to enter this study 30 days after reaching the prior studies primary endpoint Arterial anatomy not feasible for intervention based on investigator assessment Gastrointestinal Pre-existing chronic abdominal pain History of inflammatory bowel disease History of gastroparesis Prior history of gastric surgery, embolization or radiation Prior or current history of peptic ulcer disease Significant risk factors for peptic ulcer disease including daily NSAID use, active smoking or active H. Pylori infection Abnormal upper endoscopy Hepatic Cirrhosis Portal venous hypertension Hepatic Bilirubin \> 2.0 mg/dL Albumin \< 2.5 g/L Cardiovascular Known aortic pathology such as aneurysm or dissection Peripheral arterial disease Renal Renal insufficiency as evidenced by estimated GFR \< 60ml/min.1.73m2 Hematologic/Immunologic/Oncologic/Infectious Acute or chronic infection Active cancer or prior history of cancer \<10 years ago Autoimmune disease requiring immunosuppression Neutrophils \< 1.5 x 10\^9/L Platelets \< 50 x 10\^9/L INR \>1.7 Psychiatric Major diagnosed psychiatric comorbidities such a major depressive disorder, schizophrenia, bipolar disorder that are deemed to likely interfere with follow up History of an eating disorder such as anorexia or bulimia
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Adverse events | 1 year | Adverse events |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Weight | 1 year | weight change |
| Cardiovascular risk factors | 1 year | serum lipids, hemoglobin A1C, blood pressure, sleep apnea |
Outcome results
None listed