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Clinical Efficacy of Platelet Transfusion

NCT06805097 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 343

Last updated 2025-07-09

No results posted yet for this study

Summary

The aim of this study is to analyze the effect of the storage time of platelet concentrates on the occurrence of bleeding events during prophylactic platelet transfusions in patients with hematological malignancies.

Conditions

  • Thrombocytopaenia
  • Haematological Malignancies

Interventions

OTHER

Self-assessment of bleeding events

After each transfusion, the patient completes a daily bleeding event self-assessment (adapted from the WHO bleeding event scale) until the next transfusion or over a period of 10 days.

Sponsors & Collaborators

  • Centre Hospitalier Universitaire de Besancon

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-06-17
Primary Completion
2028-07-31
Completion
2028-07-31

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06805097 on ClinicalTrials.gov