The Canadian Prevention of Renal and Cardiovascular Endpoints Trial (CanPrevent)

May 9, 2022 updated by: Brendan Barrett

Canadian Collaborative Group for the Prevention of Illness in Chronic Renal Disease: The Canadian Prevention of Renal and Cardiovascular Endpoints Trial

Advanced kidney disease with it's associated heart and blood vessel problems are becoming more frequent. These problems markedly affect length and quality of life and cost a lot to treat. Treatments are known that can prevent development of advanced kidney and heart disease. These treatments are not being optimally applied in the current health system. This study aims to identify people with relatively early stage chronic kidney disease. With the participation of these people, the study will test whether a nurse coordinated clinic involving a medical kidney specialist, applying the known treatments, can reduce or delay the onset of advanced kidney disease and heart and blood vessel problems such as heart attack, stroke and death, to a greater extent than usual care. The study will also address issues of costs associated with care and illness. The nature of the care provided by the health care professionals will be studied to see how best to achieve good health outcomes.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

The pilot study is designed in two phases. The first phase is intended to provide data on some key points that need to be addressed prior to future funding applications to the CIHR and the NHLBI. These applications are currently tentatively planned for the fall of 2005. The second phase of the pilot study is intended to more completely establish the feasibility of successfully completing the full trial by examining the issue of contamination and the ability of the intervention to generate a difference between the groups with regard to use of efficacious therapies and control of modifiable risk factors, or intermediate variables on the causal pathway to the clinical end-points in the full-scale trial. The second phase will also address the need to describe the operation of the experimental intervention more thoroughly. Finally, the second phase of the pilot study will compare the randomized study groups with regard to short-term quality-of-life outcomes.

Phase1

  1. How long does it take to recruit 100 patients per study site?
  2. What recruitment strategies are most efficient?
  3. How do the baseline characteristics of those recruited compare to referred populations, and to the general population with CKD?
  4. How do the nephrologist and nurse work together to provide care to those in the intervention group?
  5. What is the nature of the care provided by the nurses and physicians to those in the intervention group?
  6. Is the study nurse able to manage the patient load?
  7. How much time and resources are needed to a) provide care, b) to carry out study measurements?
  8. Can health care resources used be measured for economic analysis?

Phase II

  1. What is the rate of loss to follow-up?
  2. What is the overall estimate of the primary outcome event rate?

  3. By one year of follow-up, what is the difference between the study groups in terms of:

    1. Protocol interventions used (estimates contamination)
    2. Proportion i) smoking; and proportion achieving ii) BP, iii) lipid, iv) diabetes, v) anemia, vi) acidosis, vii) mineral metabolism targets
    3. Quality of Life
    4. Satisfaction with care Randomized, parallel, two group, multicentre, clinical trial of people with CKD, with or without diabetes mellitus or proteinuria. The intention is to roll the pilot study into the full-scale trial if the pilot itself is deemed successful. A laboratory-based case finding method will be used preferentially to identify potential participants. This will be supplemented by practice-based case-finding approaches where necessary to ensure recruitment of a representative population. Randomization will be by a central computer-based telephone process. Stratification will be by center and presence of diabetes and proteinuria. The intervention consists of a protocol guided, multiple risk factor and chronic disease care model-like approach delivered by a trained nurse supported by a nephrologist and will be based in a nephrology clinic like setting.

Study Type

Interventional

Enrollment (Actual)

474

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Canada
    • British Columbia
      • Vancouver, British Columbia, Canada, V6Z 1Y6
        • St. Paul's Hospital
    • Newfoundland and Labrador
      • St. John's, Newfoundland and Labrador, Canada, A1B 3V6
        • Memorial University of Newfoundland
    • Nova Scotia
      • Halifax, Nova Scotia, Canada, B3H 1V8
        • Capitol District Health Authority
    • Ontario
      • London, Ontario, Canada, N6A 4G3
        • London Health Sciences Centre
    • Quebec
      • Greenfield Park, Quebec, Canada, J4V 2H1
        • Charles LeMoyne Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

40 years to 75 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Stratum 1 (expected about 50% of trial subjects): Diabetes mellitus (by clinical history with documented prior plasma glucose levels in the diabetic range, or on hypoglycemic medications) and CKD as documented by calculated (Cockroft-Gault equation) creatinine clearance between 25 and 60 mls/min/1.73m2 derived from the screening serum creatinine value and the next most recent known value from more than 2 weeks prior; OR

Stratum 2 (expected about 20% of trial subjects): Non-diabetic with CKD as defined for Stratum 1 and proteinuria of > 1g/L by dipstick in random urine at screening; OR

Stratum 3 (expected about 30% of trial subjects): Non-diabetic with CKD as defined for stratum 1, but without proteinuria as for stratum 2 at screening

Exclusion Criteria:

  • Unwilling to provide informed consent
  • Likely to die of any known existing disease within 6 months
  • Recently unstable/advanced cardiovascular disease (MI or acute coronary syndrome, hospitalized heart failure, TIA or stroke, leg amputation or gangrene in past 6 months)
  • Currently receiving active treatment for a malignant, neoplastic disease other than localized non-melanoma skin cancer
  • Progressive kidney disease currently treated by immunotherapy
  • Currently receiving dialysis or likely to do so within 6 months
  • Current organ transplant recipient (or planned within 6 months)
  • Currently receiving ongoing care for CKD, or cardiovascular disease, in a multiple intervention, disease management program.
  • Currently enrolled in another interventional trial
  • Residing in a location not amenable to follow up for the trial

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Multifactorial intervention
Nurse led clinic involving a nephrologist administering protocol driven interventions aimed at preservation of kidney function, and cardiovascular risk reduction. Blood pressure targets were specified. No specific drugs were specified. Drug classes such as primarily statins for achieving LDL targets, use of an ACE inhibitor or ARB if possible, treatment of acidosis, anemia, hyperphosphatemia, advice on smoking cessation
Other: Combined CKD and CVD Prevention
Perindopril, Lisinopril, Captopril, Candesartan, Losartan, Amlodipine, Verapamil, Chlorthalidone
Other: Cardiovascular Disease prevention
Atorvastatin, Rosuvastatin, Simvastatin, Aspirin, Clopidogrel
Other: Treatment of Chronic Kidney Disease complications
Calcitriol, Calcium carbonate, Erythropoietin, Sodium bicarbonate
Active Comparator: Usual care
Usual care includes any intervention thought appropriate by the treating family doctor and or specialists involved in the case
Other: Usual care
No prescribed intervention, just those that the patient's own family physician thought indicated

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Time to major cardiovascular event(myocardial infarction, stroke, coronary or peripheral revascularization, hospitalization for heart failure or unstable angina, or death due to cardiovascular cause)
Time Frame: 24 months
Blind expert panel determined major cardiovascular events or death
24 months
Time to first major clinical event (ESRD, non-fatal cardiovascular events as in secondary (a) or all cause death)
Time Frame: 24 months
Blind expert panel determined major cardiovascular event, death or end stage renal disease
24 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Brendan Barrett

Collaborators

University of British Columbia
Lawson Health Research Institute
Nova Scotia Health Authority
Hopital Charles Lemoyne

Investigators

  • Principal Investigator: Patrick S Parfrey, MD, Memorial University of Newfoundland
  • Principal Investigator: Brendan J Barrett, MD, Memorial University of Newfoundland

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

April 1, 2005

Primary Completion (Actual)

May 1, 2008

Study Completion (Actual)

June 1, 2008

Study Registration Dates

First Submitted

September 30, 2005

First Submitted That Met QC Criteria

October 3, 2005

First Posted (Estimate)

October 4, 2005

Study Record Updates

Last Update Posted (Actual)

May 13, 2022

Last Update Submitted That Met QC Criteria

May 9, 2022

Last Verified

May 1, 2022

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • HIC#04.154

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

Publication of study design and results in open access

IPD Sharing Time Frame

by 2011

IPD Sharing Access Criteria

Indefinite

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • CSR

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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