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NCT06740916RecruitingPhase 3

Long-term Efficacy of Once Daily Versus Twice Daily Aspirin in High-risk MPN Patients With Aspirin Resistance

Long-term Efficacy of Once Daily Versus Twice Daily Aspirin in High-risk Myeloproliferative Neoplasms Patients With Aspirin Resistance

Source: ClinicalTrials.gov · Last updated 27 Dec 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

Patients with myeloproliferative neoplasm (MPN) could have laboratory aspirin resistance and then increasing dose of aspirin from once daily to twice daily regimen is suggested. However, it is not routinely recommended to perform platelet function testing to determine aspirin resistance in MPN patients. Moreover, it is not known whether increasing dose of aspirin would always correct aspirin resistance and significantly prevent the thrombotic events in MPN patients. Therefore, this study aims to compare the efficacy of once daily versus twice daily aspirin in high-risk MPN patients with aspirin resistance. MPN patients with laboratory aspirin resistance will be included in this prospective randomized study and platelet function testing will be repeated at one and six months later. Clinical thrombosis and side effect from aspirin will be recorded for at least 2 years after intervention.

Status (registry)
Recruiting
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
240 (estimated)
First submitted
14 Dec 2024
Start date
12 Dec 2024
Primary completion date
31 Dec 2027
Lead sponsor
Siriraj Hospital
NCT number
NCT06740916

What you commit to

  • Study type: Interventional · Phase 3
  • Planned participants: 240
  • From 12 Dec 2024 to the primary completion date, 31 Dec 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Concomitant other active malignancy or cured less than 6 months
  • Receiving anticoagulant

Other illness

  • Active peptic ulcer
  • Active bleeding or Planning to undergo procedure/operation with bleeding risk

Lab values

  • Platelet count less than 50,000/microL
  • No laboratory aspirin resistance with LTA method

Who the study is looking for

  • Philadelphia negative Myeloproliferative neoplasms aged at least 18 years old

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Division of Hematology, Department of Medicine, Faculty of Medicine Siriraj Hospital
Coordinator of this site? Confirm its status
Bangkok NoiThailandRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.