Carotid Artery Stenting With Cilostazol Addition for Restenosis

NCT01261234 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 707

Last updated 2019-10-16

No results posted yet for this study

Summary

CAS-CARE study was conducted to evaluate the inhibitory effect of cilostazol, compared to that of other antiplatelet drugs, on in-stent restenosis following carotid artery stenting (CAS) in patients scheduled to undergo CAS. Study design is Multicenter Prospective Ranodomized Controlled Study, rondomized by cilostazol/non-cilostazol group prior to CAS. 900 patients will be enrolled for 2 years and followed 2 years with in-stent restenosis after CAS, evaluated by carotid ultrasound and angiography.

Conditions

  • In-stent Restenosis After Carotid Artery Stenting

Interventions

DRUG

Cilostazol or Non-Cilostazol

Cilostazol group administrate 100-200mg/day per oral, unrestricted use of other antiplatelet agents and concomitant drugs.

Sponsors & Collaborators

  • Chiba University

    collaborator OTHER
  • Nagoya University

    collaborator OTHER
  • Mie University

    collaborator OTHER
  • Wakayama Medical University

    collaborator OTHER
  • Kyoto University

    collaborator OTHER
  • Osaka University

    collaborator OTHER
  • Kobe University

    collaborator INDUSTRY
  • Foundation for Biomedical Research and Innovation

    collaborator OTHER
  • Okayama University

    collaborator OTHER
  • Yamaguchi University Hospital

    collaborator OTHER
  • Fukuoka University

    collaborator OTHER
  • Nagasaki University

    collaborator OTHER
  • Kobe City General Hospital

    lead OTHER

Principal Investigators

  • Nobuyuki Sakai, MD, DMSc · Kobe City Medical Center General Hospital

  • Hiroshi Yamagami, MD, PhD · Kobe City Medical Center General Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
45 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-12-31
Primary Completion
2019-03-31
Completion
2019-09-30

Countries

  • Japan

Study Locations

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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 NCT01261234 on ClinicalTrials.gov