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Antiplatelet Therapy for AIS Patients With Thrombocytopenia (PERSIST)

Zhejiang University logo

Zhejiang University

Status

Enrolling

Conditions

Thrombocytopenia
Acute Ischemic Stroke

Treatments

Drug: aspirin, clopidogrel, cilostazol, and dipyridamole

Study type

Interventional

Funder types

Other

Identifiers

NCT06053021
PERSIST

Details and patient eligibility

About

The goal of this clinical trial is to test the safety and effectiveness of antiplatelet therapy in acute ischemic stroke (AIS) patients with thrombocytopenia. Participants will be prescribed antiplatelet agents and followed up for 3 months.

Full description

Antiplatelet therapy is widely used in non-cardiogenic AIS patients for secondary prevention. However, it may also increase the risk of bleeding complications, especially in patients with thrombocytopenia. The goal of this clinical trial is to test the safety and effectiveness of antiplatelet therapy in acute ischemic stroke (AIS) patients with thrombocytopenia. Participants will be prescribed antiplatelet agents and followed up for 3 months.

Enrollment

1,200 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age > 18 years old
  • Acute ischemic stroke or transient ischemic attack with onset < 7 days
  • The last blood routine test before enrollment indicates platelet count < 100 x 10^9 and > 30 x 10^9

Exclusion criteria

  • Chronic renal dysfunction (GFR < 30ml/min) or severe hepatic injury
  • Indications for anticoagulation therapy, e.g. atrial fibrillation
  • Myocardial infarction within 6 months before enrollment or received percutaneous coronary intervention in the past
  • Have or plan to receive CEA or CAS in the following 3 months
  • Life expectancy less than 1 year
  • Plan to receive invasive surgery in the following 3 months and have high risk of uncontrollable bleeding
  • Pregnant or lactating women
  • Individuals identified by researchers as unsuitable for participation in the study due to other reasons.

Trial design

Primary purpose

Prevention

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

1,200 participants in 1 patient group

Intervention
Experimental group
Description:
Participants will be prescribed antiplatelet agents including aspirin, clopidogrel, cilostazol, and dipyridamole.
Treatment:
Drug: aspirin, clopidogrel, cilostazol, and dipyridamole

Trial contacts and locations

1

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Central trial contact

Min Lou, PhD

Data sourced from clinicaltrials.gov

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