Trials / Completed
CompletedNCT01460966
Assessment of Distal Protection Device in Patients at High Risk for Distal Embolism in Acute Coronary Syndrome (ACS)
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 200 (actual)
- Sponsor
- Yokohama City University Medical Center · Academic / Other
- Sex
- All
- Age
- —
- Healthy volunteers
- Not accepted
Summary
Attenuated plaque ≥ 5mm by intravascular ultrasound(IVUS) was reported to be high risk for distal embolism in Acute coronary syndrome(ACS). The purpose of this study is to assess the effect of thrombus aspiration catheter and distal protection device (filter wire; Filtrap™) in the aforementioned subgroup of patients at high risk for distal embolism.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Filtrap™ + Thrombus aspiration catheter | Combination of distal protection device (Filtrap™ )and thrombus aspiration catheter |
| PROCEDURE | Thrombus aspiration catheter | Thrombus aspiration catheter only |
Timeline
- Start date
- 2012-07-01
- Primary completion
- 2015-12-23
- Completion
- 2017-01-31
- First posted
- 2011-10-27
- Last updated
- 2017-04-20
Locations
1 site across 1 country: Japan
Source: ClinicalTrials.gov record NCT01460966. Inclusion in this directory is not an endorsement.