Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Class |
|---|---|
| Population Health Research Institute | OTHER |
| St. Joseph's Healthcare Hamilton | OTHER |
Not provided
Not provided
Not provided
Not provided
Pilot multicentre, open-label, parallel-arm randomized controlled trial (RCT) of 60 patients to demonstrate the feasibility of enrolling patients with high-risk cardiovascular disease (CVD) into an RCT of bariatric surgery versus medical weight management (MWM).
STUDY OBJECTIVE The primary objective of this pilot study is to assess the feasibility of an RCT of bariatric surgery compared to MWM in patients with morbid obesity and high-risk CVD. If we can demonstrate that this trial is feasible, the next step would be to conduct a large-scale RCT to evaluate the efficacy of bariatric surgery for the reduction of cardiovascular complications in this patient population.
STUDY AIMS:
STUDY HYPOTHESES Study enrollment will be feasible at a rate of at least 1.25 patients per centre per month. Timely delivery of the intervention is possible, with >80% of patients undergoing bariatric surgery within 30 days of randomization. The rate of crossover between the control and intervention arms will be low at <2.5% per year. 30-day mortality rates in the intervention group will be comparable to that of an age and gender matched cohort without CVD who had bariatric surgery at the 2 study sites during the study period.
DESIGN The present study is a multicentre, open-label, parallel-arm feasibility RCT with blinded endpoint assessment (PROBE design) of bariatric surgery compared to MWM in patients with morbid obesity and high-risk CVD.
Individuals who meet study eligibility criteria will be randomized in 1:1 fashion to bariatric surgery (intervention arm) or MWM (control arm). Bariatric surgery will consist of laparoscopic Roux-en-Y gastric bypass or sleeve gastrectomy, performed at the discretion of the surgeon and according to local standards.
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Intervention | Active Comparator | Bariatric surgery will consist of laparoscopic Roux-en-Y gastric bypass or sleeve gastrectomy performed at the discretion of the surgeon and according to local standards. |
|
| Control | No Intervention | Medical Weight Management (MWM) corresponds to the standard medical practice for weight loss that is available at the local participating centre, and thus reflects the local standard of care. |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Bariatric surgery | Procedure | Although there may be slight variation by centre, Gastric Bypass generally involves creation of a 30-50 cc stomach pouch, which is anastamosed with a Roux limb of jejunum 75-100 cm in length and a biliary limb of 20-30 cm in length. The operation creates a small gastric pouch, with nutrients bypassing the duodenum and proximal jejunum. Sleeve Gastrectomy involves decreasing the size of the stomach to approximately 15% of its original size by resecting a large portion of the stomach along the greater curvature. |
| Measure | Description | Time Frame |
|---|---|---|
| Recruitment rate | Recruitment rate (target of 60 patients over 24 months or 1.25 patients per centre per month) | 24 months (or when recruitment is complete) |
| Time to intervention administration | Target of bariatric surgery performed within 30 days of randomization in >80% | 30 days |
| Crossover rate | Crossover rate between control and intervention arm | At study completion (an average of 1.5 years follow-up) |
| Measure | Description | Time Frame |
|---|---|---|
| Change in weight at 1 year | Change in weight in kilograms at 1 year | 12 months |
| Change in BMI at 1 year | BMI (kg/m^2) will be calculated using weight in kg at 1 year, and height |
Not provided
Inclusion Criteria:
Body mass index >35 kg/m2
Age ≥18 years
High-risk CVD, defined as the presence of any one of the following:
Patient is deemed eligible to undergo bariatric surgery according to local practice guidelines
Exclusion Criteria:
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Tara McCready, PhD, MBA | Contact | 905-521-2100 | tara.mccready@phri.ca | |
| Wanna Fong | Contact | 905-521-2100 | wanna.fong@phri.ca |
| Name | Affiliation | Role |
|---|---|---|
| Jorge Wong, MD MPH FRCPC | PHRI, Hamilton Health Sciences, McMaster University | Principal Investigator |
| Aristithes Doumouras, MD MPH FRCSC | St. Joseph's Healthcare, McMaster University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| St. Joseph's Healthcare Hamilton | Recruiting | Hamilton | Ontario | L8N 4A6 | Canada |
Not provided
| Label | URL |
|---|---|
| Population Health Research Institute | View source |
| St. Joseph's Heathcare Hamilton Bariatric Surgery Program | View source |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| ID | Term |
|---|---|
| D009767 | Obesity, Morbid |
| D002318 | Cardiovascular Diseases |
| ID | Term |
|---|---|
| D009765 | Obesity |
| D050177 | Overweight |
| D044343 | Overnutrition |
| D009748 | Nutrition Disorders |
Not provided
Not provided
| ID | Term |
|---|---|
| D050110 | Bariatric Surgery |
| ID | Term |
|---|---|
| D049088 | Bariatrics |
| D000073319 | Obesity Management |
| D013812 | Therapeutics |
| D013514 | Surgical Procedures, Operative |
Not provided
Not provided
Individuals who meet study eligibility criteria will be randomized in 1:1 fashion to bariatric surgery (intervention arm) or MWM (control arm).
Not provided
Not provided
Not provided
Not provided
|
| 12 months |
| Composite outcome of cardiovascular mortality, myocardial infarction (MI), stroke and hospitalization for heart failure (HF) | Composite outcome of cardiovascular mortality, myocardial infarction, stroke and hospitalization for heart failure | 12 months, and through study completion (an average of 1.5 years follow-up) |
| Change in percent excess weight loss (%) at 1 year | Excess weight loss is a standard outcome measure in obesity research. It is calculated as the percentage of excess body weight lost after surgery. Excess body weight (kg) is calculated as current weight (kg) minus ideal body weight (kg) for a given height. Ideal body weight (kg) is taken from standardized tables. | 12 months |
| Change in New York Heart Association (NYHA) Functional Classification at 1 year | NYHA Class is a standardized classification system for severity of heart failure symptoms, and ranges from class I to class IV, with IV being the most severe symptoms and class. | 12 months |
| Change in 6-minute walk test distance (m) at 1 year | The 6 Minute Walk Test is an exercise test used to assess aerobic capacity and endurance. The distance covered over a time of 6 minutes is used as the outcome. Longer distances indicate better performance. | 12 months |
| Change in 36-Item Short Form Survey (SF-36) questionnaire score at 1 year | The SF-36 is a measure of health-related quality-of-life. It includes eight health domains: physical functioning (10 items), bodily pain (2 items), role limitations due to physical health problems (4 items), role limitations due to personal or emotional problems (4 items), emotional well-being (5 items), social functioning (2 items), energy/fatigue (4 items), and general health perceptions (5 items). Scores for each domain range from 0 to 100, with a higher score defining a more favorable health state. | 12 months |
| Change in EuroQuol (EQ-5D-5L) quality of life questionnaire score at 1 year | EQ-5D-5L is a standardized instrument for measuring health status, which includes a descriptive system asking about 5 health dimensions as well as an evaluation of overall health status with a visual analogue scale. The descriptive system comprises five dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 5 levels from which respondents choose one response: no problems, slight problems, moderate problems, severe problems and extreme problems. The visual analogue scale asks individuals to mark their health status on the day of the interview on a 20 cm vertical scale with end points of 0 and 100. Zero corresponds to " the worst health you can imagine", and 100 corresponds to "the best health you can imagine". | 12 months |
| Number of participants with new onset Atrial Fibrillation (AF) at 1 year | Will determine the number of participants who receive a new clinical diagnosis of AF during the study follow-up. | 12 months, and through study completion (an average of 1.5 years follow-up) |
| D009750 |
| Nutritional and Metabolic Diseases |
| D001835 | Body Weight |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |