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Choice of Anticoagulant for Primary Hemostasis Studies With PFA200® (Platelet Function Analyser)

Choice of Anticoagulant for Primary Hemostasis Studies With PFA200® (Platelet Function Analyser)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06753838
Acronym
BAPAPFA
Enrollment
100
Registered
2024-12-31
Start date
2025-01-21
Completion date
2025-12-31
Last updated
2025-09-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hemostasis

Brief summary

The PFA (platelet function analysis) test is prescribed for the exploration of primary hemostasis and the study of platelet-willebrand factor interaction. It is performed using citrated blood, with technical difficulties and frequent alarms that may be linked to the choice of anticoagulant (citrate). It is proposed to compare the results obtained with a conventional citrate tube and a BAPA tube, which is an anticoagulant used in clinical research and which blocks coagulation by another mechanism that would have less impact on blood platelets.

Interventions

BIOLOGICALSampling of 3 additional BAPA tubes

the 3 additional tubes will be taken at the same time as the blood sample taken for the routine PFA test

Sponsors

Centre Hospitalier Universitaire Dijon
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Person having given their non-opposition * Person of legal age * Person receiving a haemostasis consultation at the haemophilia and haemorrhagic diseases treatment center followed by a blood sample with a PFA test prescribed by the doctor (the test is not added for the study).

Exclusion criteria

* persons under legal protection (curatorship, guardianship) * persons subject to a court protection order * pregnant, parturient or breast-feeding women * adult incapable or unable to give consent * minor

Design outcomes

Primary

MeasureTime frameDescription
Occlusion time measurementat baselineMeasurement of the occlusion times of the 2 cartridges (collagen/ADP and collagen/epinephrine) with the classic 0.109M citrate tube and the BAPA tube, with any PLC alarms and observation of the stained blood smears.

Countries

France

Contacts

Primary ContactEmmanuel De Maistre
emmanuel.demaistre@chu-dijon.fr03 80 29 32 57

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026