DRUG
bivalirudin
Bivalirudin; 0.75mg/kg/h IV bolus followed immediately by 1.75 mg/kg/h infusion for the duration of the procedure
Status
Withdrawn
Phase
Phase 4
Enrollment
0
Locations
1
Results
Not posted
Publications
0
Study summary
To monitor the frequency of the development of thrombocytopenia in patients with Heparin Induced Thrombocytopenia/Heparin Induced Thrombocytopenia and Thrombosis Syndrome receiving bivalirudin during Percutaneous Coronary Intervention
Interventions
DRUG
Bivalirudin; 0.75mg/kg/h IV bolus followed immediately by 1.75 mg/kg/h infusion for the duration of the procedure
Timeline
First posted
Sep 25, 2008
Study start
Sep 2008
Primary completion
Sep 2009
Study completion
May 10, 2010
Results posted
Not reported
Registry updated
Oct 19, 2020
Outcomes
Platelet counts
Time frame · 6, 12, 24, 48 Hours
Not reported in the indexed record.
Eligibility
Inclusion Criteria: * Clinically Documented History of HIT/HITTS * Suspicion of HIT/HITTS Exclusion Criteria: * Bleeding Diathesis * Ischemic Stroke * Chronic Thrombocytopenia * Hematologic Malignancy * Contraindication to bivalirudin * Pregnant or nursing mothers
Study locations
United States. Showing up to 24 locations stored in the fast local snapshot.
Duke Clinical Research Institute
Durham, North Carolina, United States
Publications
No PMID-linked publications were present in this registry snapshot.
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