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Clinical Trial Details — Status: Completed

Administrative data

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

Study information

Verified date November 2019
Source Maisonneuve-Rosemont Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.


Description:

The remaining factor in determining the effectiveness of bariatric surgery in the transplant population will be to study the effect on the pharmacokinetics of immunosuppressive medication, height, weight, BMI, abdominal circumference, blood pressure, Hba1c , average daily insulin requirements, lipid profile, TSH, 24h urine creatinine clearance and the SF-36 Quality of life questionnaire.


Recruitment information / eligibility

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

Study Design


Intervention

Procedure:
laparoscopic sleeve gastrectomy


Locations

Country Name City State
Canada MaisonneuveRH Montréal Quebec

Sponsors (3)

Lead Sponsor Collaborator
Maisonneuve-Rosemont Hospital Astellas Pharma Canada, Inc., Canadian surgical research fund

Country where clinical trial is conducted

Canada, 

Outcome

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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