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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01665729
Other study ID # 2011-2-48
Secondary ID
Status Recruiting
Phase N/A
First received August 12, 2012
Last updated August 14, 2012
Start date June 2011
Est. completion date December 2015

Study information

Verified date August 2012
Source Third Affiliated Hospital, Sun Yat-Sen University
Contact Zhengqi Lu, prof.
Phone 86 13570102668
Email lzq1828@yahoo.com.cn
Is FDA regulated No
Health authority China: Ministry of Science and Technology
Study type Observational

Clinical Trial Summary

Negligence or contempt of the etiology and pathogenesis of minor ischaemic stroke in the early diagnosis and effective treatment leads to more than 40-50% of patient with recurrent episodes, and 10% patient died. Therefore, diagnosis and treatment of minor ischaemic stroke according to the etiology and pathogenesis is important.

The 2007 Korean modified TOAST type got some progress, but there exists two major disadvantages: imperfect diagnosis and pathogenesis of perforator artery infarction etiology; lack of typing according to the pathogenesis of large atherosclerotic infarction and taking measures of treatment according to the new types. Recently, domestic professor Gaoshan proposes new approach to diagnose and treat minor ischaemic stroke according to the etiology and pathogenesis of CISS typing, but the pathogenesis of hypoperfusion infarction with severe stenosis of large artery is unclear. Is it low perfusion? Or artery-artery embolization? Or both? How to distinguish the pathogenesis of branch artery disease: by atherosclerosis? Or hyalinosis? Or both? How to check the validity of clinical types? This study take different interventions according to different types and observation of the long term clinical results of intervention( mortality, recurrence rate, disability rate and rate of cerebral hemorrhage and subarachnoid hemorrhage), in order to clarify the new types can indeed solve the current problem of minor ischaemic stroke with high mortality, recurrence rate, disability rate and rate of cerebral hemorrhage and subarachnoid hemorrhage.


Recruitment information / eligibility

Status Recruiting
Enrollment 1000
Est. completion date December 2015
Est. primary completion date August 2012
Accepts healthy volunteers No
Gender Both
Age group 20 Years to 79 Years
Eligibility Inclusion Criteria:

one of two conditions:

1. conscious patients with any of NIHSS score = 1,or

2. NIHSS = 3

Exclusion Criteria:

- patients Over 80 years of age

- patients With serious heart, lung, liver, kidney dysfunction or

- severe systemic complications,

- a known tumor,

- pregnancy,

- having a history of cerebral hemorrhage

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
China Department of Neurology,The Third Af?liated Hospital of Sun yat-sen University Guangzhou Guangdong

Sponsors (1)

Lead Sponsor Collaborator
Li Haiyan

Country where clinical trial is conducted

China, 

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