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Diagnostic Test
Diagnostic algorithm for Heparin Induced Thrombocytopenia (HIT Trial)
N/A
Waitlist Available
Led By Lisa Duffett, MSc, MD
Research Sponsored by Ottawa Hospital Research Institute
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Patient with clinical suspicion of HIT by treating physician
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 2 years
Awards & highlights
HIT Trial Summary
This trial is testing a new method for diagnosing HIT, which is a blood clotting disorder.
Eligible Conditions
- Heparin Induced Thrombocytopenia
HIT Trial Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowHIT Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 2 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~2 years
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
False negative management failures
Recruitment
Secondary outcome measures
Death
Major arterial and venous thromboembolism events
Myocardial infarction
+4 moreHIT Trial Design
1Treatment groups
Experimental Treatment
Group I: diagnostic algorithmExperimental Treatment1 Intervention
Optimizing the interpretation of the more readily available anti-PF4 assay would reduce the reliance on functional testing/ confirmatory testing (Serotonin Release Assay, SRA) and the number of patients exposed to unnecessary changes in anticoagulation therapy while awaiting the timely functional test results
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Who is running the clinical trial?
Ottawa Hospital Research InstituteLead Sponsor
561 Previous Clinical Trials
2,785,511 Total Patients Enrolled
Lisa Duffett, MSc, MDPrincipal InvestigatorOttawa Hospital Research Institute
Frequently Asked Questions
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