OPT-CAD Score GUIded Dual ANtiplatelet De-esCalation Time

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-80
SponsorShenyang Northern Hospital

About this trial

Monotherapy with a P2Y12 inhibitor after a minimum period of DAPT following percutaneous coronary intervention (PCI) is an emerging de-escalation antiplatelet strategy in recent years. However, the optimal timing for de-escalating DAPT in ACS patients undergoing PCI remains debated. The OPT-CAD score is a risk stratification tool derived from Chinese patients which has been demonstrated superior predictive capabilities for ischemic events and all-cause mortality than the GRACE score. Therefore, we hypothesize that the OPT-CAD score can be used to guide the timing of the DAPT de-escalation strategy to monotherapy with P2Y12 inhibitors for ACS patients, that is, low-risk patients could be de-escalated after 1 month, while high-risk patients could be de-escalated after 3 months, so as to achieve individualized antithrombotic therapy and maximize patient benefit.

Eligibility criteria

Qualifiers

Adult patients with ages of 18-80 years;

Patients with clinically diagnosed ACS who have undergone at least one DES implantation;

Individuals capable of completing the OPT-CAD scoring calculation;

Researchers assessing that participants can tolerate at least a 12-month duration of DAPT therapy;

Disqualifiers

Left main coronary artery lesion PCI;

Allergy to study drugs such as aspirin, clopidogrel, or ticagrelor;

Meeting 1 major or 2 minor criteria for high bleeding risk according to the ARC-HBR criteria;

Anticipated need for revascularization or surgical intervention within 12 months;

Trial design

Treatments tested in this trial

  • standard DAPT
  • OPT-CAD score guided DAPT de-escalation

Treatment groups

3,490 Participants
are divided into 2 treatment groups

Sponsors and collaborators