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NCT06216821Not yet recruiting

OPT-CAD Score GUIded Dual ANtiplatelet De-esCalation Time

OPT-CAD Score Guided Dual Antiplatelet De-escalation Time in Patients With Acute Coronary Syndrome Undergoing Undergoing Percutaneous Coronary Intervention: a Register-based Randomized Controlled Study
Shenyang Northern HospitalClinicalTrials.govdrug
Study focus
Drug/Device/Intervention
standard DAPT
Study type
Interventional
Intervention type
drug
Sponsor & location
Primary sponsor
Shenyang Northern Hospital
Location
Shenyang, China
Timeline & enrollment
Phase
N/A
Start date
Feb 01, 2024
End date
Dec 31, 2025
Enrollment
3490 participants
Primary outcome

Net adverse clinical events (NACE)

Summary

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.

ICD-10 classifications
Acute myocardial infarctionAcute myocardial infarction, unspecifiedAcute subendocardial myocardial infarctionAcute ischaemic heart disease, unspecifiedOther acute ischaemic heart diseases
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT06216821
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT06216821 through Pure Global AI's free database. This phase not specified trial is sponsored by Shenyang Northern Hospital and is currently Not yet recruiting. The study focuses on Acute Coronary Syndrome. Target enrollment is 3490 participants.

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