Obesity, Morbid Clinical Trial
Official title:
Prospective, Clinical Study of the Effect of Bariatric Surgery, Laparoscopic Sleeve Gastrectomy, on the Pharmacokinetics of Immunosuppressive Drugs in the Morbidly Obese, Kidney Transplant Candidate
NCT number | NCT01913392 |
Other study ID # | 2014-530-13022 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | July 18, 2013 |
Est. completion date | May 2018 |
Verified date | November 2019 |
Source | Maisonneuve-Rosemont Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
A prospective clinical trial will study the effects of laparoscopic sleeve gastrectomy in the potential renal transplant candidate who is denied acceptance due mainly to the morbid obesity.
Status | Completed |
Enrollment | 15 |
Est. completion date | May 2018 |
Est. primary completion date | May 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - adult (>18 years) - stage IV and V chronic renal disease (glomerular filtration rate < 30 ml/min, - body mass index (BMI) of greater than 40 kg/m2 or > 35 with at least one co-morbidity such as hypertension, dyslipidemia or diabetes Exclusion Criteria: - medically unfit for surgical intervention - previous gastric or intestinal surgery - active gastric disease - pregnancy or lactation - known intolerance to tacrolimus or mycophenolic acid - awaiting potential multi-organ transplantation - active infection |
Country | Name | City | State |
---|---|---|---|
Canada | MaisonneuveRH | Montréal | Quebec |
Lead Sponsor | Collaborator |
---|---|
Maisonneuve-Rosemont Hospital | Astellas Pharma Canada, Inc., Canadian surgical research fund |
Canada,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | changes in the pharmacokinetics of oral immunosuppressive medications due to bariatric surgery, comparing pre-bariatric surgery to 12 months post-operative | Tacrolimus and Mycophenolate AUC 0-24h | pre-bariatric surgery and 1 year after surgery | |
Primary | degree of weight loss achieved after bariatric surgery in the chronic renal failure patient. | weight, BMI and abdominal circumference measures | baseline and every 3 months | |
Primary | Evaluate the change in general quality of life score, SF-36 | comparison of the SF score between Baseline and month 3, Baseline and month 6 and Baseline and month 12 | Baseline and 1 year after bariatric surgery | |
Secondary | evaluate changes to residual renal function in the pre-dialysis renal transplant candidate | serum creatinine/ urea, sodium, potassium, magnesium, calcium, phosphate and bicarbonate pre surgery and month 12 | at baseline versus month 12 post-bariatric surgery | |
Secondary | evaluate the change in the number and dose of medications required to treat co-morbidities including, hypertension, hyperlipidemia and diabetes mellitus | concommitant medication records at baseline vs month 12 | baseline and 12 month post-bariatric surgery | |
Secondary | the incidence of complications post-bariatric surgery will be evaluated | non serious and serious adverse events collection at Baseline, month 6 and month 12 | 1, 6 and 12 months post-bariatric surgery |
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