STrategies for Anticoagulation in Patients With thRombocytopenia and Cancer-associated Thrombosis
Launched by OTTAWA HOSPITAL RESEARCH INSTITUTE · Feb 15, 2022
Trial Information
Current as of November 13, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying the best way to treat patients with cancer who have blood clots and low platelet counts. Blood clots are common in cancer patients, and they are usually treated with blood thinners, which help prevent more clots. However, if a patient has a low number of platelets—cells that help stop bleeding—they are at a higher risk of bleeding when using blood thinners. The trial will include 50 adult patients with cancer, diagnosed with a blood clot in the last 14 days and with platelet counts below 50,000. Participants must be able to provide consent and have had recent cancer treatment.
In this pilot study, participants will be randomly assigned to receive either a full dose of blood thinners along with a platelet transfusion or a lower dose of blood thinners without the transfusion. The study will follow patients for 90 days to see which treatment works better. If successful, this research could lead to a larger trial that will help determine the safest and most effective treatment strategies for patients with cancer, low platelets, and blood clots. This is an important step in improving care for these patients.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 1. Adult patients (age ≥ 18) with active malignancy (malignancy diagnosed or treated within the previous 6 months, or progressive/relapsed);
- • 2. Objectively confirmed VTE within last 14 days for which therapeutic anticoagulation is planned;
- • 3. Thrombocytopenia with a platelet count \< 50,000/uL from cancer therapy or malignancy itself;
- • 4. Able to provide written informed consent
- Exclusion Criteria:
- • 1. Receipt of anticoagulant for index VTE with platelet count \< 50,000/uL for \> 72 hours;
- • 2. Superficial vein thrombosis only;
- • 3. Life expectancy \< 1 month (as judged by the treating physicians);
- • 4. Creatinine clearance \< 30 ml/min;
- • 5. Contraindication to LMWH such as a history of heparin induced thrombocytopenia;
- • 6. Thrombocytopenia from other causes, such as thrombotic microangiopathy, immune thrombocytopenia, disseminated intravascular coagulation;
- • 7. Previously documented history of refractoriness to platelet transfusion secondary to HLA antibodies;
- • 8. Refusal of blood products;
- • 9. Anticoagulation at any dose is deemed unsafe (i.e. active bleeding or bleeding disorders)
About Ottawa Hospital Research Institute
The Ottawa Hospital Research Institute (OHRI) is a leading academic research institute dedicated to advancing health and healthcare through innovative research and evidence-based practices. Affiliated with The Ottawa Hospital and the University of Ottawa, OHRI fosters a collaborative environment that brings together clinicians, scientists, and trainees to conduct groundbreaking clinical trials and translational research. With a focus on improving patient outcomes, OHRI specializes in a wide range of fields, including cancer, cardiovascular health, and regenerative medicine. The institute is committed to ethical research practices and the dissemination of knowledge to enhance public health and inform healthcare policy.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Edmonton, Alberta, Canada
Ottawa, Ontario, Canada
Windsor, Ontario, Canada
Patients applied
Trial Officials
Tzu-Fei Wang, MD
Principal Investigator
Ottawa Hospital Research Institute
Marc Carrier, MD
Principal Investigator
Ottawa Hospital Research Institute
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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