Kidney Transplant Failure

NCT01296061 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 270

Last updated 2019-09-06

No results posted yet for this study

Summary

Primary Hypotheses:

1. Among patients who retain the failed kidney transplant, those who continue immunosuppressant medication will have more deaths than patients who discontinue these drugs
2. Among patients who retain the failed kidney transplant, those who continue immunosuppressant medication will have more hospitalizations for sepsis than patients who discontinue these drugs
3. Among patients who retain the failed kidney transplant, those who continue immunosuppressant medication will have fewer rejection events than patients who discontinue these drugs

Secondary Hypotheses:

1. Patients who undergo elective nephrectomy (to remove the failed kidney transplant) will have fewer deaths than those who retain the failed kidney transplant
2. Patients who undergo elective nephrectomy (to remove the failed kidney transplant) will have fewer hospitalizations for sepsis than those who retain the failed kidney transplant
3. Among patients who retain the failed kidney transplant, those who continue immunosuppressant medication will have lower levels of allosensitization (anti-HLA antibodies) than those who discontinue these drugs
4. Patients who undergo elective nephrectomy will have higher levels of allosensitization (anti-HLA antibodies) than patients who retain the failed kidney transplant

Conditions

  • Acute Graft Rejection
  • Renal Failure Chronic Requiring Dialysis

Sponsors & Collaborators

  • Canadian Institutes of Health Research (CIHR)

    collaborator OTHER_GOV
  • St. Paul's Hospital, Canada

    collaborator OTHER
  • Vancouver General Hospital

    collaborator OTHER
  • Kingston Health Sciences Centre

    collaborator OTHER
  • University of Saskatchewan

    collaborator OTHER
  • University of Calgary

    collaborator OTHER
  • University of Manitoba

    collaborator OTHER
  • University Health Network, Toronto

    collaborator OTHER
  • Unity Health Toronto

    collaborator OTHER
  • St. Joseph's Healthcare Hamilton

    collaborator OTHER
  • London Health Sciences Centre

    collaborator OTHER
  • McGill University Health Centre/Research Institute of the McGill University Health Centre

    collaborator OTHER
  • Maisonneuve-Rosemont Hospital

    collaborator OTHER
  • Centre hospitalier de l'Université de Montréal (CHUM)

    collaborator OTHER
  • CHU de Quebec-Universite Laval

    collaborator OTHER
  • University of Alberta

    collaborator OTHER
  • Ottawa Hospital Research Institute

    lead OTHER

Principal Investigators

  • Greg Knoll, MD · U of Ottawa, The Ottawa Hospital, OHRI

  • John Gill, MD · UBC, St Paul's Hospital Vancouver, BC

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-08-31
Primary Completion
2016-10-31
Completion
2017-07-31

Countries

  • Canada

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01296061 on ClinicalTrials.gov