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Optimal anti-platelet therapy in elderly patients with acute coronary syndromes undergoing percutaneous coronary intervention

A prospective, single-center, randomized, parallel-group study on the efficacy of low-dose ticagrelor dual anti-platelet therapy on elderly patients with acute coronary syndromes undergoing percutaneous coronary intervention

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200062478
Enrollment
Unknown
Registered
2022-08-08
Start date
2022-08-08
Completion date
Unknown
Last updated
2023-04-12

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

Conditions

Acute Coronary Syndrome

Interventions

Low dose ticagrelor group:Ticagrelor 90 mg bid + aspirin 100 mg qd was maintained until 1 month after PCI, and after 1 month, it was changed to ticagrelor 60 mg bid + aspirin 100 mg qd until 1 year af
Standard dose ticagrelor group:Ticagrelor 90 mg bid + aspirin 100 mg qd was maintained until 1 year after PCI.
Clopidogrel group:Clopidogrel 75mg qd + aspirin 100mg qd maintained for 1 year after PCI.

Sponsors

Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Age greater than or equal to 65 years old; 2. Diagnosed with ACS; 3. Coronary artery disease confirmed by angiography and intended for PCI.

Exclusion criteria

Exclusion criteria: 1. Contraindications for coronary intervention; 2. Plan to use other ADP receptor blockers; 3. Long-term anticoagulation; 4. Known bleeding tendency or coagulation disorder; 5. History of intracranial hemorrhage; 6. Central nervous system tumor or intracranial vascular abnormalities (such as aneurysm, arteriovenous malformation); 7. Intracranial or spinal cord surgery within 5 years; 8. Gastrointestinal bleeding within the past 6 months or within the past 30 days Major surgery; 9. History of previous ischemic stroke; 10. Risk of bradycardia events (eg, sick sinus syndrome or second/third-degree atrioventricular block) unless permanent pacemaker therapy has been received; 11. Severe liver disease; 12. Renal failure requiring dialysis; 13. Combined with malignant tumor or other end-stage diseases that seriously affect survival; 14. Participated in other clinical studies within the past 30 days.

Design outcomes

Primary

MeasureTime frame
Adenosine diphosphate-induced platelet-fibrin clot strength, MAADP;

Secondary

MeasureTime frame
ADP-induced platelet inhibition rate;Platelet-fibrin clot strength, MA;Platelet aggregation rate;Composite endpoint of MACCE, including all-cause death, non-fatal MI, stent thrombosis, non-fatal stroke, target vessel revascularization;Composite endpoint of all bleeding events, including BARC bleeding definition types 1, 2, 3, and 5.;Adverse events such as drug-related dyspnea, bradycardia, syncope;

Countries

China

Contacts

Public ContactJie Zhao

Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College

fwzhaojie@126.com+86 13911036089

Outcome results

None listed

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