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Starting soon Observational

Pilot Study to Establish a Repertoire of Megakaryocyte Markers, Quantifiable by Spectral Flow Cytometry, in Bone Marrow and Circulating in Patients Undergoing Cardiac Surgery for Bypass Grafting

NCT07026851 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2025-07
Last updated
2025-06-18

Condition(s) studied

Cardiac Surgery for Bypass Grafting

Investigational drug(s) / intervention(s)

Blood and bone marrow sampling

Blood and bone marrow sampling: This intervention involves the collection of peripheral blood before and 3 days after coronary artery bypass grafting (CABG), as well as a one-time collection of bone marrow sample during sternotomy. Samples are analyzed using spectral flow cytometry to characterize the phenotype and maturation stages of circulating and medullary megakaryocytes using a panel of specific surface antibodies.

Study summary

Megakaryopoiesis, the mechanism of blood platelet production, is difficult to assess in clinical practice as it relies solely on microscopic description. Recent studies described the presence of emergency megakaryopoiesis bypassing the classical maturation stages under certain conditions. Circulating megakaryocytes were identified in inflammatory and hemostatic conditions. The aim of this study is to characterize the phenotype of medullar and circulating megakaryocytes by flow cytometry during and after coronary artery bypass grafting.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: \- Age over 18 * Indication for programmed cardiac surgery, specifically coronary artery bypass grafting with sternotomy * Up to date social security coverage * Patients able to understand the purpose and constraints of the research project Exclusion Criteria: * Refusal to participate in the study, * Pregnant and/or breastfeeding women (clinical interview), * Unscheduled cardiac surgery, Acquired hematologic disorders (acute leukemia, lymphomas, myelodysplastic syndromes, and myeloproliferative syndromes) * Treatment with thrombopoietin receptor agonists * Treatment with anti-inflammatory (included corticoids) or/and immunosuppressors * Hematopoietic stem cell transplantation or organ transplantation * Active cancer with or without treatment (in remission, ongoing or treated within the last 6 months), * Palliative care patients * Any other type of cardiac surgery and previous sternotomy, * History of external thoracic radiotherapy, * Patient under legal protection (curatorship, guardianship or safeguard of justice) * Patients with ongoing clinical trial requiring collection of additional blood or bone marrow samples

Primary outcome measure(s)

  • Phenotype of bone marrow and circulating megakaryocytes — Day of surgery
    Circulating and bone marrow megakaryocytes will be analyzed using spectral flow cytometry on samples collected during coronary artery bypass surgery. Cells will be labeled with a panel of specific surface antibodies . Megakaryocytes will be classified by maturation stage (multipotent progenitor \[MPP\], common myeloid progenitor \[CMP\], megakaryocyte-erythrocyte progenitor \[MEP\], pro-megakaryocyte \[proMK\], immature megakaryocyte \[imMK\], mature megakaryocyte \[MK\]) and specialization status (specialized MKs).

Trial sites (1)

FacilityCityRegionStatus
Toulouse University Hospital Toulouse France
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07026851 on ClinicalTrials.gov ↗ ← All trials in France