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A randominzed controlled trial of Antiplatelet therapy after clopidogre stopping on PCI patients

A randominzed controlled trial of Antiplatelet therapy after clopidogre stopping on PCI patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-09000337
Enrollment
Unknown
Registered
2009-01-04
Start date
2009-03-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

coronary heart disease patients who underwent primary PCI with stenting

Interventions

Group A:Stop clopidogrel directly, only aspirin 100mg/d
Group B:Aspirin 200mg/d for three months, and then decease
Group C:the first month: clopidogrel 75mg/qod
the second month: clopidogrel 75mg, every three days
the third month: clopidogrel 75mg, every four days
the fourth month: stop clopidogrel, during clopidogrel decrement, aspirin 100mg/d will be taken
Group D:to continue clopidogrel 75mg/d+ aspirin 100mg/d for 3 months, and then stop clopidogrel, only aspirin 100mg/d

Sponsors

The Fourth Affiliated Hospital of Guangxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: patients who underwent primary PCI with stenting

Exclusion criteria

Exclusion criteria: patients who regularly had clopidogrel, hypersusceptible to aspirin and clopidogrel, with a history of alimentary tract hemorrhage, bleeding diathesis, platelet dysfunction, had an adverse event while receiving clopidogrel therapy, PT>1.5 controlled, platelet count <10*10^9/L, hemoglobin <90 g/L.

Design outcomes

Primary

MeasureTime frame
cardiovascular events;Mortality, AMI;

Secondary

MeasureTime frame
platelet aggregation, CRP, P-selectin, haemorrhage;

Countries

China

Contacts

Public ContactYang Fan
wzyyfgh99820@yahoo.c+86 0 13617810565

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026