Actively Recruiting

Phase 2
Age: 18Years +
All Genders
NCT05820126

Cold Versus Room Temperature Storage of Platelets for Bleeding in Hematologic Malignancy - a Pilot Trial

Led by Ottawa Hospital Research Institute · Updated on 2025-07-31

50

Participants Needed

1

Research Sites

84 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This is a pilot trial to discover the feasibility of recruiting 50 pts over the course of 12 months. The trial is testing the efficacy of using cold-stored vs. room temperature stored (current standard of care) platelets to treat bleeding in persons with hematological disorders and thrombocytopenia.

CONDITIONS

Official Title

Cold Versus Room Temperature Storage of Platelets for Bleeding in Hematologic Malignancy - a Pilot Trial

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult patients aged 18 or older admitted to Malignant Hematology ward with hematologic malignancy or marrow aplasia, including those undergoing chemotherapy, immunotherapy, hematopoietic stem cell transplant, or admitted for symptom management
  • Moderate thrombocytopenia with platelet count between 10 and 100 x 10⁹/L
  • Platelet transfusion ordered to treat bleeding
Not Eligible

You will not qualify if you...

  • Severe thrombocytopenia with platelet count less than 10 x 10⁹/L
  • Known platelet refractoriness requiring HLA or HPA selected platelet concentrates
  • International normalized ratio (INR) greater than 2.0
  • Activated partial thromboplastin time (aPTT) greater than 40 seconds
  • Receiving therapeutic anticoagulation (unfractionated heparin, low molecular weight heparin, warfarin, direct oral anticoagulant)
  • Known congenital bleeding disorder
  • History of unprovoked venous thromboembolic disease
  • Platelet transfusion for grade 2 or higher bleeding in the past 24 hours
  • Order for multiple platelet transfusions at once
  • Refusal of blood transfusion
  • Prior participation in CoVeRTS-HM trial
  • Participation in other clinical trials with interventions affecting CoVeRTS-HM treatment or outcomes
  • Unable or unwilling to provide informed consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

The Ottawa Hospital - General Campus

Ottawa, Ontario, Canada, K1H 8L6

Actively Recruiting

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Research Team

J

Johnathan M Mack, MD

CONTACT

A

Alan Tinmouth, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

2

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