The Safety and Efficacy of Cilostazol in Ischemic Stroke Patients With Peripheral Arterial Disease (SPAD Study)

NCT01188824 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 801

Last updated 2013-10-07

No results posted yet for this study

Summary

The purpose of this study is to investigate the Safety and Efficacy of Cilostazol in slowing down the progression of peripheral arterial disease (PAD) in ischemic stroke patients with PAD in Taiwan.

Conditions

Interventions

DRUG

Cilostazol

100 mg, bid p.o.

OTHER

placebo

1 tablet, bid

Sponsors & Collaborators

  • National Taiwan University Hospital

    collaborator OTHER
  • Shin Kong Wu Ho-Su Memorial Hospital

    collaborator OTHER
  • Tri-Service General Hospital

    collaborator OTHER
  • Far Eastern Memorial Hospital

    collaborator OTHER
  • Changhua Christian Hospital

    collaborator OTHER
  • Chi Mei Medical Hospital

    collaborator OTHER
  • National Cheng-Kung University Hospital

    collaborator OTHER
  • Kaohsiung Medical University Chung-Ho Memorial Hospital

    collaborator OTHER
  • E-DA Hospital

    collaborator OTHER
  • Mackay Memorial Hospital

    collaborator OTHER
  • Cathay General Hospital

    collaborator OTHER
  • En Chu Kong Hospital

    collaborator OTHER
  • Kuang Tien General Hospital

    collaborator OTHER
  • Chung Shan Medical University

    collaborator OTHER
  • Taipei Veterans General Hospital, Taiwan

    collaborator OTHER_GOV
  • China Medical University Hospital

    lead OTHER

Principal Investigators

  • Chung Y. Hsu, MD. Ph.D. · China Medical University Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
50 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-09-30
Primary Completion
2013-07-31
Completion
2013-07-31

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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 NCT01188824 on ClinicalTrials.gov