Skip to content

Performance Evaluation of the Biological Diagnosis of HIT

Performance Evaluation of the Biological Diagnosis of Heparin-induced Thrombocytopenia (HIT)

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06180785
Acronym
HIT
Enrollment
894
Registered
2023-12-22
Start date
2022-06-27
Completion date
2023-12-31
Last updated
2023-12-22

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

Conditions

Heparin-induced Thrombocytopenia (HIT)

Keywords

Heparin-induced thrombocytopenia, HIT, heparin therapy, heparin treatments, molecular weight heparin, IgG antibodies, platelet factor 4 (PF4), heparin complex, thrombotic risk

Brief summary

Heparin-induced thrombocytopenia (HIT) is a severe complication of heparin therapy with a non-negligible incidence (estimated at 2.6% of unfractionated heparin treatments and 0.2% of low molecular weight heparin treatments). It is generally secondary to the appearance of IgG antibodies directed against the platelet factor 4 (PF4) - heparin complex. These antibodies, once bound to this complex, are likely to activate platelets: the thrombotic risk generated can be potentially fatal.

Interventions

None listed

Sponsors

University Hospital, Strasbourg, France
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

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

Inclusion criteria

: * Adult patient (≥ 18 years of age) * Hospitalized at HUS between 01/01/2009 and 31/12/2019 * Specimen sent to the HUS Hematology Laboratory for biological diagnosis of HIT between 01/01/2009 and 31/12/2019 * Data collected by the CRPV and analyzed by the HIT multidisciplinary group in order to reach a consensus decision on the presence or absence of HIT * Patient does not object to the reuse of his medical data for scientific research purposes.

Exclusion criteria

* Patient for whom no test has been performed at the HUS Hematology Laboratory * Patient for whom no data has been collected by the CRPV * Patient for whom the HIT group could not confirm or deny the presence of HIT

Design outcomes

Primary

MeasureTime frame
Retrospective description of the biological diagnosis approach for heparin-induced thrombocytopenia (HIT) in the Hematology laboratory of the University Hospitals of Strasbourgthrough study completion, an average of 1 month

Countries

France

Contacts

Primary ContactAgathe HERB, PharmD
agathe.herb@chru-strasbourg.fr33 3 88 12 75 53

Outcome results

None listed

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