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OpenTrials
Recruiting

NCT Number: NCT07302087

Platelet Serotonin Deficiencies: the Strasbourg Experience

Hemorrhagic syndromes are investigated using algorithms established by reference centers and hemostasis societies.

The investigation of platelet dense granules (nucleotide and serotonin testing) is part of the second-line tests.

It can be performed in cases of platelet aggregation abnormalities in platelet-rich plasma (PRP) suggesting a secretion abnormality, or in cases where the latter is normal, it can be performed if the patient's clinical presentation points to a primary hemostasis abnormality and the clinician wishes to pursue further investigations Intraplatelet serotonin deficiencies are often iatrogenic and may be accompanied by bleeding.

Their impact on platelet function is poorly documented.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Centre de Ressources et de Compétences des Maladies Hémorragiques Constitutionnelles - CHU de Strasbourg - France

Strasbourg, 67091, France

Location status: Recruiting

Location contact

AMANDINE ROBERT, MD

SUB_INVESTIGATOR

ARNAUD DUPUIS, MD

SUB_INVESTIGATOR

DIHIA CHEBBAH, MD

SUB_INVESTIGATOR

Dominique Desprez, MD

CONTACT

[email protected]

33 3 88 12 83 71

Dominique Desprez, MD

PRINCIPAL_INVESTIGATOR

LAURENT SATTLER, MD

PRINCIPAL_INVESTIGATOR

OLIVIER FEUGEAS, MD

SUB_INVESTIGATOR

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adult patient (≥ 18 years old)
  • Treated at Strasbourg University Hospital for a hemorrhagic syndrome, suggesting a primary hemostasis abnormality and normal von Willebrand factor, during the period from January 1, 2023, to April 1, 2024.

Exclusion criteria

  • Refusal to participate in the study

Treatment and study plan

Primary outcomes

  1. Score of ISTH BAT Hemorrhagic Questionnaire

    Time frame: Up to 12 months

    ISTH BAT bleeding questionnaire with its 12-item grid scored from 0 to 4:

    A score ≥ 4 in men or ≥ 6 in women makes the presence of a constitutional hemostasis disorder highly probable

Study contacts

Contact information is provided by the study sponsor or research team.

Dominique DESPREZ, MD

CONTACT

[email protected]

33 3 88 12 83 71

Sponsors and collaborators

Lead sponsor

University Hospital, Strasbourg, France

Other

Registry information

Acronym: SEROTSTG

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
Dec 24, 2025
Registry last updated
Dec 24, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.