Trials / Unknown
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
| Type | Name | Description |
|---|---|---|
| DRUG | Aspirin | Discontinuation of aspirin at 3 months after the Ultimaster sirolimus-eluting stent implantation by the physician's discretion. |
| DRUG | Thienopyridine | Discontinuation 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.