Skip to content

ASPirin in Immune thRombocytopenia Patients With Cardiovascular disEase

ASPirin in Immune thRombocytopenia Patients With Cardiovascular disEase

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04912505
Acronym
ASPIRE
Enrollment
4
Registered
2021-06-03
Start date
2023-01-16
Completion date
2024-01-02
Last updated
2025-12-31

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

Conditions

Purpura, Thrombocytopenic

Keywords

Immune thrombocytopenia, aspirin, pharmacodynamics, proof-of-concept study

Brief summary

The incidence of immune thrombocytopenia increases with older age. This population is at risk for arterial thrombosis. Due to an increased turn-over of platelets, low-dose aspirin once daily may be insufficient in this population to protect against arterial thrombosis. This study is aimed at assessing the pharmacodynamics of aspirin once daily on platelet function in these patients.

Detailed description

The incidence of immune thrombocytopenia increases with older age. About 20% of patients who develop immune thrombocytopenia are exposed to low-dose aspirin for arterial thrombosis prophylaxis. Moreover, immune thrombocytopenia patients have an increased risk for developing arterial thrombosis as compared with matched controls from the general population. Because ITP patients have an increased turn-over of platelets and aspirin is an irreversible inhibitor of cyclooxygenase-1, aspirin taken once daily may be insufficient to provide stable inhibition of platelet function. This has been demonstrated in myeloproliferative neoplasms with a higher platelet turn-over as well; aspirin is given twice daily to these patients. In immune thrombocytopenia, epidemiological findings sustain this assumption because aspirin is not associated to an increased risk of bleeding. The primary aim of this study is to assess the residual platelet function after 75 mg aspirin intake (H24). Secondary objectives are to assess the kinetics of platelet function after daily 75 mg aspirin intake and the relation with arterial thrombosis.

Interventions

DRUGAspirin

Run-in phase during one week with daily aspirin intake at 8 AM; visit 1: blood sampling at H24 and H2; intermediate phase (two weeks): daily aspirin intake at 8 PM; visit 2: blood sampling at H12; then daily intake of aspirin at the time preferred by the patient and study end visit 2 weeks after visit 2

Sponsors

University Hospital, Toulouse
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Intervention model description

Single arm with sequential variations of daily aspirin intake time

Eligibility

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

Inclusion criteria

* adult patients * non-treated immune thrombocytopenia or immune thrombocytopenia with stable treatment (at least 1 month) * treated with aspirin daily for a cardiovascular disease; stable platelet count \< 100 x 109/L * at least one month following an arterial thrombosis * no other antiplatelet drug and anticoagulant * female patient with childbearing potential must have acceptable method of birth control * affiliated or benefiting from public health insurance

Exclusion criteria

* opposition to participate * adults under guardianship or other legal protection * deprived of their liberty by judicial or administrative decision * pregnancy or breastfeeding

Design outcomes

Primary

MeasureTime frameDescription
Thromboxane B224 hoursPlatelet production of thromboxane B2 24 hours after a 75 mg aspirin intake

Countries

France

Outcome results

None listed

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