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ShorT and OPtimal duration of Dual AntiPlatelet Therapy-2 study

ShorT and OPtimal duration of Dual AntiPlatelet Therapy-2 study - ShorT and OPtimal duration of Dual AntiPlatelet Therapy-2 study(STOPDAPT-2)

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000019948
Enrollment
3000
Registered
2015-11-27
Start date
2015-12-25
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Coronary Heart Disease, Angina Pectoris, Myocardial Infarction

Interventions

After PCI with Xience, dual antiplatelet therapy (DAPT) will be performed for one month. Following that, clopidogrel monotherapy will be continued up to 5 years after index PCI (1-month DAPT group) Af

Sponsors

Kyoto University, Graduate School of Medicine, Department of Cardiovascular Medicine
Lead Sponsor
Research Institute for Production Development
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients who have undergone PCI with the everolimus-eluting cobalt-chromium stent (EES, XienceTM) 2. Patients who have not experienced major complications (death, MI, stroke, or major bleeding) during hospital stay for treatment 3. Patients who are capable of oral dual antiplatelet therapy consisting of aspirin and a P2Y12 receptor antagonist

Exclusion criteria

Exclusion criteria: 1. Patients requiring oral anticoagulants 2. Patients with medical history of intracranial hemorrhage 3. Patients who have experienced serious complications (MI, stroke, and major bleeding) during hospital stay post-PCI 4. Patients with DES other than Xience implanted in PCI performed at the time of enrollment 5. Patients confirmed to have no tolerability to clopidogrel before enrollment 6. Patients requiring continuous administration of antiplatelet drugs (PDE3 inhibitors, prostaglandin preparations, etc.) other than aspirin and P2Y12 receptor inhibitors (prasugrel, clopidogrel, and ticlopidine) at the time of enrollment 7. Patients with coronary bioabsorbable vascular scaffold (BVS) implanted prior to or at the time of enrollment

Design outcomes

Primary

MeasureTime frame
The composite of cardiovascular death, myocardial infarction (MI), stroke (ischemic and hemorrhagic), stent thrombosis (Definite stent thrombosis yet to develop into MI), and severe bleeding (TIMI Major/Minor) at 12 months after index PCI.

Secondary

MeasureTime frame
Cardiovascular death, MI, Stroke, ARC definite ST, Major bleeding (TIMI Major/ Minor) at 12 months after index PCI. Cardiovascular death, MI, Stroke, ARC definite ST, Major bleeding (TIMI Major/ Minor), Upper gastrointestinal endoscopy / upper gastrointestinal endoscopic treatment at 60 months after index PCI.

Countries

Japan

Contacts

Public ContactHirotoshi Watanabe

Kyoto University, Graduate School of Medicine Department of Cardiovascular Medicine

hwatanab@kuhp.kyoto-u.ac.jp075-751-4255

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026