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UnknownNCT02837003

3-Month Discontinuation of Dual Antiplatelet Therapy After Ultimaster Sirolimus-Eluting Stent Implantation

Status
Unknown
Phase
Study type
Observational
Enrollment
1,500 (estimated)
Sponsor
Teikyo University · Academic / Other
Sex
All
Age
20 Years
Healthy volunteers
Not accepted

Summary

To evaluate safety of reduction of dual antiplatelet therapy period to three months after implantation of Ultimaster sirolimus-eluting stent (U-SES). Additionally to investigate appropriateness of thienopyridine monotherapy with discontinuation of aspirin.

Conditions

Interventions

TypeNameDescription
DRUGAspirinDiscontinuation of aspirin at 3 months after the Ultimaster sirolimus-eluting stent implantation by the physician's discretion.
DRUGThienopyridineDiscontinuation of thienopyridine at 3 months after the Ultimaster sirolimus-eluting stent implantation by the physician's discretion.

Timeline

Start date
2016-07-01
Primary completion
2019-03-01
Completion
2019-03-01
First posted
2016-07-19
Last updated
2016-08-02

Locations

1 site across 1 country: Japan

Source: ClinicalTrials.gov record NCT02837003. Inclusion in this directory is not an endorsement.

3-Month Discontinuation of Dual Antiplatelet Therapy After Ultimaster Sirolimus-Eluting Stent Implantation (NCT02837003) · Clinical Trials Directory