Current partner codePEPTIDESDE
NCT00759083·Phase 4·INTERVENTIONAL

Bivalirudin PCI Registry in Heparin Induced Thrombocytopenia/Heparin Induced Thrombocytopenia and Thrombosis Syndrome (HIT/HITTS) Patients

Status

Withdrawn

Phase

Phase 4

Enrollment

0

Locations

1

Results

Not posted

Publications

0

Study summary

What the protocol is testing.

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

Treatment arms and agents.

DRUG

bivalirudin

Bivalirudin; 0.75mg/kg/h IV bolus followed immediately by 1.75 mg/kg/h infusion for the duration of the procedure

Timeline

From registration to results.

  1. First posted

    Sep 25, 2008

  2. Study start

    Sep 2008

  3. Primary completion

    Sep 2009

  4. Study completion

    May 10, 2010

  5. Results posted

    Not reported

  6. Registry updated

    Oct 19, 2020

Outcomes

What the study measures.

Primary outcomes

Platelet counts

Time frame · 6, 12, 24, 48 Hours

Secondary outcomes

Not reported in the indexed record.

Eligibility

Who can take part.

Minimum age
18 Years
Maximum age
Not reported
Sex
ALL
Healthy volunteers
No

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

1 registered sites.

United States. Showing up to 24 locations stored in the fast local snapshot.

Duke Clinical Research Institute

Durham, North Carolina, United States

Publications

Results and literature.

No PMID-linked publications were present in this registry snapshot.

Primary links

Continue at the source.

Related trials

More studies on Bivalirudin.

Related PeptideStat pages

Put the record in context.

Research pages describe evidence. Vendor pages, where available, describe independently tracked research-product listings and are not clinical recommendations.