Cardiovascular Diseases Clinical Trial
— ESTTERODOfficial title:
A One-Year, Prospective, Randomized, Controlled Study Evaluating The Efficacy Of Switching From The Twice Daily Tacrolimus Formulation To The Extended Release, Once Daily Formulation To Reduce The Framingham Cardiovascular Risk Scores.
Verified date | January 2018 |
Source | University of Saskatchewan |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Current standard prophylactic immunosuppression in renal transplantation includes tacrolimus,
a calcineurin inhibitor, dosed twice daily. In Canada, oral tacrolimus has been available as
a twice daily formulation marketed as Prograf® since 1997. It has recently become available
in an extended release formulation called Advagraf®, which is dosed once daily. Advagraf® has
been demonstrated to be therapeutically equivalent to Prograf® in the renal transplant
maintenance population, and as a result it has been is approved as an alternative to the
twice daily formulation in these patients. There is an evolving and expanding positive
clinical experience with Advagraf® in kidney transplantation and it has shown to be preferred
by many patients, due to the diminished dosing frequency. In clinical trials, Advagraf® has
been shown to have other potential benefits over Prograf® such as less inter and
intra-patient variability, improved cardiovascular profiles, and improved kidney function.
Compared to Prograf®, Advagraf® also has a lower Cmin or 'trough' concentration as well as a
lower Cmax or 'peak' concentration. The purpose of this study is to convert stabilized renal
transplant patients currently receiving Prograf® to Advagraf®, to investigate these potential
therapeutic benefits.
The Framingham Risk Score and the Reynold's Risk Score are currently recommended by the
Canadian Cardiovascular Society (CCS) to predict 10-year cardiovascular risk in the general
population. Surrogate markers are widely used in clinical trials to shorten follow-up
durations. In this study, the investigators will use the Framingham Risk Score and Reynold's
Risk Score to quantify changes in estimated cardiovascular risk. The investigators also
intend to examine novel inflammatory markers to investigate cardiovascular risk.
The investigators hypothesize that the more consistent drug exposure and lower Cmax noted
with Advagraf® will decrease Framingham Risk Score, Reynolds Risk score as well as markers of
inflammation in kidney transplant recipients.
Status | Completed |
Enrollment | 36 |
Est. completion date | December 2017 |
Est. primary completion date | December 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 74 Years |
Eligibility |
Inclusion Criteria: - Kidney transplant patients currently stable on the twice-daily formulation and who are followed as outpatients. - Stability is defined as change in serum creatinine of less than 10% over the last two months - Age 18-74 years old - At least six months after transplantation - Lack of rejection within the last 12 weeks - Serum creatinine less than 300 umol/L at enrolment - Negative urine pregnancy test for female patients of childbearing potential - Consent to the study - Not included in a clinical trial within the last 90 days Exclusion Criteria: - Patients with other types of solid organ transplants - Patients with any form of substance abuse or psychiatric disorder. - Patients with acute or chronic diarrhea - Patients receiving anti-lymphocyte treatment for rejection within the last six months - Patients on cyclosporine and or not receiving a mycophenolate derivative. - Patients with significant liver disease defined as having an elevated bilirubin by at least two times the upper value of the normal range - Patients who have any unstable medical condition that could interfere with the study - Patients with chronic viral infection with HIV, Hep C and HCV. - Presence of any acute illness requiring admission to the hospital for the last 4 weeks - Pregnancy - Significant cardiovascular event such as MI, stroke or TIA within the last 12 weeks or uncontrolled hypertension. - Immunosuppressant changes within the last month. |
Country | Name | City | State |
---|---|---|---|
Canada | St Paul's Hospital | Saskatoon | Saskatchewan |
Lead Sponsor | Collaborator |
---|---|
University of Saskatchewan | Astellas Pharma Canada, Inc. |
Canada,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in the Framingham risk scores and change in the Reynolds Risk Score. | Visit 1, Visit 3 (12 months) | ||
Secondary | Comparison in GFR between the two groups. | Visit 1, Visit 3 (12 months) | ||
Secondary | Effect of therapy on CV biomarkers, insulin resistance and lipid profile. | CV biomarkers will be assessed by luminex and insulin resistance and lipid profile will be assessed by the Metabolic Syndrome | Visit 1, Visit 3 (12 months) | |
Secondary | To look at change in the glomerular filtration rate (GFR) over the duration of the study. | Vist 1, Visit 3 (12 months) |
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT05654272 -
Development of CIRC Technologies
|
||
Recruiting |
NCT05650307 -
CV Imaging of Metabolic Interventions
|
||
Recruiting |
NCT04515303 -
Digital Intervention Participation in DASH
|
||
Completed |
NCT04056208 -
Pistachios Blood Sugar Control, Heart and Gut Health
|
Phase 2 | |
Recruiting |
NCT04417387 -
The Genetics and Vascular Health Check Study (GENVASC) Aims to Help Determine Whether Gathering Genetic Information Can Improve the Prediction of Risk of Coronary Artery Disease (CAD)
|
||
Not yet recruiting |
NCT06211361 -
Cardiac Rehabilitation Program in Patients With Cardiovascular Disease
|
N/A | |
Not yet recruiting |
NCT06032572 -
Evaluation of the Safety and Effectiveness of the VRS100 System in PCI (ESSENCE)
|
N/A | |
Recruiting |
NCT04514445 -
The BRAVE Study- The Identification of Genetic Variants Associated With Bicuspid Aortic Valve Using a Combination of Case-control and Family-based Approaches.
|
||
Enrolling by invitation |
NCT04253054 -
Chinese Multi-provincial Cohort Study-Beijing Project
|
||
Completed |
NCT03273972 -
INvestigating the Lowest Threshold of Vascular bENefits From LDL Lowering With a PCSK9 InhibiTor in healthY Volunteers
|
N/A | |
Completed |
NCT03680638 -
The Effect of Antioxidants on Skin Blood Flow During Local Heating
|
Phase 1 | |
Recruiting |
NCT04843891 -
Evaluation of PET Probe [64]Cu-Macrin in Cardiovascular Disease, Cancer and Sarcoidosis.
|
Phase 1 | |
Completed |
NCT04083846 -
Clinical Study to Investigate the Pharmacokinetic Profiles and Safety of High-dose CKD-385 in Healthy Volunteers(Fed)
|
Phase 1 | |
Completed |
NCT04083872 -
Clinical Study to Investigate the Pharmacokinetic Profiles and Safety of Highdose CKD-385 in Healthy Volunteers(Fasting)
|
Phase 1 | |
Completed |
NCT03466333 -
Postnatal Enalapril to Improve Cardiovascular fUnction Following Preterm Pre-eclampsia
|
Phase 2 | |
Completed |
NCT03619148 -
The Incidence of Respiratory Symptoms Associated With the Use of HFNO
|
N/A | |
Completed |
NCT03693365 -
Fluid Responsiveness Tested by the Effective Pulmonary Blood Flow During a Positive End-expiratory Trial
|
||
Completed |
NCT04082585 -
Total Health Improvement Program Research Project
|
||
Completed |
NCT05132998 -
Impact of a Comprehensive Cardiac Rehabilitation Program Framework Among High Cardiovascular Risk Cancer Survivors
|
N/A | |
Completed |
NCT05067114 -
Solutions for Atrial Fibrillation Edvocacy (SAFE)
|