Carotid Artery Stenting With Cilostazol Addition for Restenosis
NCT01261234 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 707
Last updated 2019-10-16
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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