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Assessment of Distal Protection Device in Patients at High Risk for Distal Embolism in Acute Coronary Syndrome (ACS)

NCT01460966 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 200

Last updated 2017-04-20

No results posted yet for this study

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

PROCEDURE

Filtrap™ + Thrombus aspiration catheter

Combination of distal protection device (Filtrap™ )and thrombus aspiration catheter

PROCEDURE

Thrombus aspiration catheter

Thrombus aspiration catheter only

Sponsors & Collaborators

  • Teikyo University

    collaborator OTHER

  • Yokohama City University Medical Center

    lead OTHER

Principal Investigators

  • Kiyoshi Hibi, Doctor · Yokohama City Universiy Medical Center

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-07-31
Primary Completion
2015-12-23
Completion
2017-01-31

Countries

  • Japan

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01460966 on ClinicalTrials.gov