MDS-CAN: A Prospective National MDS Clinical Database and Local Tissue Bank

NCT02537990 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 1200

Last updated 2016-11-16

No results posted yet for this study

Summary

The purposes of this study are: 1. To identify and quantify the health utilities and quality of life experienced by patients who have been diagnosed with MDS and what are their predictors. 2. Measure the effects of patient related factors like frailty and comorbidity on quality of life and overall survival or toxicity to therapy. 3. Assess how quality of life changes over time and what are its predictors. This will be valuable information that may guide therapy, transfusion practices, etc., as MDS is a chronic, incurable disease that is often progressive.

Conditions

  • Myelodysplastic Syndrome (MDS)

Sponsors & Collaborators

  • Tom Baker Cancer Centre

    collaborator OTHER
  • CancerCare Manitoba

    collaborator OTHER
  • The Ottawa Hospital

    collaborator OTHER
  • Princess Margaret Hospital, Canada

    collaborator OTHER
  • Jewish General Hospital

    collaborator OTHER
  • Health Sciences Centre, Winnipeg, Manitoba

    collaborator OTHER
  • British Columbia Cancer Agency

    collaborator OTHER
  • Providence Health & Services

    collaborator OTHER
  • Vancouver Coastal Health

    collaborator OTHER_GOV
  • Juravinski Cancer Center

    collaborator OTHER
  • Réseau de Santé Vitalité Health Network

    collaborator OTHER
  • Royal Victoria Hospital, Canada

    collaborator OTHER
  • Capital Health, Canada

    collaborator OTHER
  • Saskatoon City Hospital

    collaborator OTHER
  • Sunnybrook Health Sciences Centre

    lead OTHER

Principal Investigators

  • Rena Buckstein, MD FRCPC · Sunnybrook Health Science Centre

Eligibility

Min Age
19 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-08-31
Primary Completion
2020-02-29
Completion
2020-02-29

Countries

  • Canada

Study Locations

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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 NCT02537990 on ClinicalTrials.gov