PFA 100 Evaluation and Reference Interval HOACNY
Launched by HEMATOLOGY ONCOLOGY ASSOCIATES OF CENTRAL NEW YORK · Oct 19, 2023
Trial Information
Current as of June 26, 2025
Enrolling by invitation
Keywords
ClinConnect Summary
No description provided
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Age 18 years or older
- • Able to consent to study
- • Exclusion Criteria from entire study
- • Primary hemostasis diagnosis
- • Von Willebrand Disease
- • Bernard-Soulier syndrome
- • Glanzmann thrombasthenia
- • Idiopathic thrombocytopenic purpura
- • Drug-induced thrombocytopenia
- • Heparin-induced thrombocytopenia
- • Thrombotic thrombocytopenic purpura
- • Hemolytic uremic syndrome
- • Participant is on anticoagulant therapy
- • Specifically thienopyrdines \[Ticlopidine, Clopidogrel\] and GPIIb/IIIa inhibitors \[ReoPro, Aggrastat, Integrilin\]
- • Participant is on medication that contains ASA or aspirin (see list below in Study Procedure)
- • Participant is on nonsteroidal anti-inflammatory agents that are known to induce temporary platelet dysfunction (see list below in Study Procedure)
- • Participant is on non-prescription medications containing aspirin (see list below in Study Procedure)
- • PFA-100 result falls outside of reference interval listed in the package insert (suggested criteria in the PFA-100 Evaluation Protocol as described in the PFA-100 System: Getting Started Guide)
- • If hematocrit is less than 35%
- • If platelets are less than 150 x10\^3/uL
- • Exclusion Criteria from Cohort B but not Cohort A
- • Potential for adverse reactions between current medication and aspirin as dictated by staff pharmacist
- • Allergy to ASA or aspirin
- • Previous allergic reaction to ASA or aspirin
- • Participant is pregnant
- • Asthma, or history of, with nasal polyps and rhinitis
- • Stomach ulcers or bleeding
- • Severe kidney disease
- • Severe liver disease
- • Hemophilia
- • Pregnant or breast feeding
About Hematology Oncology Associates Of Central New York
Hematology Oncology Associates of Central New York is a distinguished clinical trial sponsor dedicated to advancing the field of cancer treatment through innovative research and patient-centered care. Comprising a team of experienced hematologists and oncologists, the organization focuses on conducting high-quality clinical trials that aim to evaluate novel therapies and improve outcomes for patients with hematologic and oncologic conditions. Committed to excellence in patient safety and ethical standards, the associates leverage cutting-edge technology and comprehensive care models to contribute valuable insights to the medical community while fostering a supportive environment for participants throughout their treatment journey.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
East Syracuse, New York, United States
Patients applied
Trial Officials
Theresa O'Sullivan, BS,MLT(ASCP)
Principal Investigator
Employee
Steven Duffy, MD
Study Director
Physician
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported