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Evaluation of Argatroban Injection in Pediatric Patients Requiring Anticoagulant Alternatives to Heparin

Phase 4
Completed
Conditions
Thrombocytopenia
Thrombosis
Registration Number
NCT00039858
Lead Sponsor
Encysive Pharmaceuticals
Brief Summary

The purpose of this study is to evaluate the safe and effective dose of Argatroban for prophylaxis and/or treatment of thrombosis in pediatric patients with current or previous diagnosis of heparin-induced thrombocytopenia (HIT) and thrombosis syndrome (HITTS), or who in the opinion of the investigator require alternative anticoagulation due to an underlying condition.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
24
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (13)

Children's Hospital of Orange County

🇺🇸

Orange, California, United States

Mattel Children's Hospital at UCLA

🇺🇸

Los Angeles, California, United States

Children's Hospital of Boston

🇺🇸

Boston, Massachusetts, United States

Michigan Congenital Heart Center

🇺🇸

Ann Arbor, Michigan, United States

Primary Children's Medical Center

🇺🇸

Salt Lake City, Utah, United States

Rush University Medical Center

🇺🇸

Chicago, Illinois, United States

University of Chicago Children's Hospital

🇺🇸

Chicago, Illinois, United States

Children's Hospital of Illinois

🇺🇸

Peoria, Illinois, United States

Rainbow Babies at Children's Hospital

🇺🇸

Cleveland, Ohio, United States

Oregon Health & Science University

🇺🇸

Portland, Oregon, United States

Children's Hospital of Philadelphia

🇺🇸

Philadelphia, Pennsylvania, United States

Kosair Children's Hospital, University of Louisville

🇺🇸

Louisville, Kentucky, United States

Children's Hospital and Regional Medical Center

🇺🇸

Seattle, Washington, United States

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