Stroke Imaging Package Study of Intracranial Atherosclerosis ( SIPS-ICAS )

NCT03719820 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 550

Last updated 2020-03-31

No results posted yet for this study

Summary

A prospective, multicenter, cohort study to explore the stroke mechanisms of symptomatic intracranial atherosclerosis, the dynamic changes under aggressive medical treatment and their associations with clinical events using conventional MRI sequences plus high-resolution magnetic resonance (HR-MRI).

Conditions

  • Acute Ischemic Stroke AIS
  • Intracranial Atherosclerosis ICAS

Interventions

DRUG

aggressive medical management

Aspirin (100 mg daily) and Clopidogrel (75 mg daily) for 3 months and Rosuvastatin (20mg daily) for at least 6 months as well as traditional risk factors management

Sponsors & Collaborators

  • Peking Union Medical College Hospital

    collaborator OTHER
  • General Hospital of Chinese Armed Police Forces

    collaborator OTHER
  • General Hospital of Shenyang Military Region

    collaborator OTHER
  • Subei People's Hospital of Jiangsu Province

    collaborator OTHER
  • Fujian Medical University Union Hospital

    collaborator OTHER
  • Tangshan Gongren Hospital

    collaborator OTHER
  • Third Affiliated Hospital, Sun Yat-Sen University

    collaborator OTHER
  • Qingdao Municipal Hospital

    collaborator OTHER
  • West China Hospital

    collaborator OTHER
  • Shanghai Tong Ren Hospital

    collaborator OTHER
  • Ruijin Hospital

    collaborator OTHER
  • The First Affiliated Hospital of University of South China

    collaborator OTHER
  • JiNing NO.1 People Hospital

    collaborator UNKNOWN
  • Tongji Hospital

    collaborator OTHER
  • The University of HongKong-Shenzhen Hospital

    collaborator UNKNOWN
  • Beijing Anzhen Hospital

    collaborator OTHER
  • Beijing Hospital

    collaborator OTHER_GOV
  • Peking University International Hospital

    collaborator OTHER
  • Beijing Tongren Hospital

    collaborator OTHER
  • China-Japan Friendship Hospital

    collaborator OTHER
  • Peking University First Hospital

    collaborator OTHER
  • Beijing Friendship Hospital

    collaborator OTHER
  • Beijing Chao Yang Hospital

    collaborator OTHER
  • Qilu Hospital of Shandong University (Qingdao)

    collaborator OTHER
  • Shandong Provincial Hospital

    collaborator OTHER_GOV
  • The Second Hospital of Hebei Medical University

    collaborator OTHER
  • Hebei General Hospital

    collaborator OTHER
  • First Affiliated Hospital of Zhejiang University

    collaborator OTHER
  • China-Japan Union Hospital, Jilin University

    collaborator OTHER
  • Zhejiang Provincial Tongde Hospital

    collaborator OTHER
  • People's Hospital of Ningxia Hui Autonomous Region

    collaborator OTHER
  • Taiyuan Central Hospital of Shanxi Medical University

    collaborator OTHER
  • Hong Xinglong Central Hospital

    collaborator UNKNOWN
  • Changzhi People's Hospital

    collaborator OTHER
  • Weihai Municipal Hospital

    collaborator OTHER
  • Southwest Hospital, China

    collaborator OTHER
  • Affiliated Taihe Hospital of Hubei University of Medicine

    collaborator UNKNOWN
  • Nanshi Hospital of Nanyang

    collaborator UNKNOWN
  • Wei-Hai Xu

    lead OTHER

Principal Investigators

  • Weihai Xu, MD · Peking Union Medical College Hospital

Eligibility

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

Timeline & Regulatory

Start
2018-11-14
Primary Completion
2020-12-31
Completion
2021-06-30

Countries

  • China

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 NCT03719820 on ClinicalTrials.gov