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ASPirin in Immune thRombocytopenia Patients With Cardiovascular disEase (ASPIRE)

Primary Purpose

Purpura, Thrombocytopenic

Status
Recruiting
Phase
Phase 2
Locations
France
Study Type
Interventional
Intervention
Aspirin
Sponsored by
University Hospital, Toulouse
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Purpura, Thrombocytopenic focused on measuring Immune thrombocytopenia, aspirin, pharmacodynamics, proof-of-concept study

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Toulouse HospitalRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Single arm

Arm Description

Sequential variations of daily aspirin intake time

Outcomes

Primary Outcome Measures

Thromboxane B2
Platelet production of thromboxane B2 24 hours after a 75 mg aspirin intake

Secondary Outcome Measures

Full Information

First Posted
May 28, 2021
Last Updated
July 27, 2023
Sponsor
University Hospital, Toulouse
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1. Study Identification

Unique Protocol Identification Number
NCT04912505
Brief Title
ASPirin in Immune thRombocytopenia Patients With Cardiovascular disEase
Acronym
ASPIRE
Official Title
ASPirin in Immune thRombocytopenia Patients With Cardiovascular disEase
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Recruiting
Study Start Date
January 16, 2023 (Actual)
Primary Completion Date
January 1, 2025 (Anticipated)
Study Completion Date
September 1, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Toulouse

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Purpura, Thrombocytopenic
Keywords
Immune thrombocytopenia, aspirin, pharmacodynamics, proof-of-concept study

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Model Description
Single arm with sequential variations of daily aspirin intake time
Masking
None (Open Label)
Allocation
N/A
Enrollment
10 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Single arm
Arm Type
Experimental
Arm Description
Sequential variations of daily aspirin intake time
Intervention Type
Drug
Intervention Name(s)
Aspirin
Intervention Description
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
Primary Outcome Measure Information:
Title
Thromboxane B2
Description
Platelet production of thromboxane B2 24 hours after a 75 mg aspirin intake
Time Frame
24 hours

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Guillaume MOULIS, MD PhD
Phone
05 61 77 58 94
Ext
33
Email
moulis.g@chu-toulouse.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Guillaume MOULIS, MD PhD
Organizational Affiliation
University Hospital, Toulouse
Official's Role
Principal Investigator
Facility Information:
Facility Name
Toulouse Hospital
City
Toulouse
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Guillaume MOULIS, MD

12. IPD Sharing Statement

Plan to Share IPD
No

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ASPirin in Immune thRombocytopenia Patients With Cardiovascular disEase

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