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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05882123
Other study ID # 20220642
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 2014
Est. completion date December 2015

Study information

Verified date May 2023
Source The First Hospital of Hebei Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The investigators continuously collected data from 482 AIS inpatients at the Neurology Department of Hebei General Hospital. Both demographic and clinical data were collected from the study subjects. Different head magnetic resonance imaging sequences were used to assess the subjects' CMBs, white matter lesions, and old lacunar infarcts (LI). Various statistical methods, including the t-test, χ2 test, and logistic regression, were used to analyze the gender heterogeneity of the influencing factors for CMBs in AIS patients.


Recruitment information / eligibility

Status Completed
Enrollment 482
Est. completion date December 2015
Est. primary completion date December 2015
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Aged 18 years and older - Must meet the diagnostic criteria for AIS as presented in the Chinese Guidelines for Diagnosis and Treatment of Acute Ischemic Stroke 2014 - Must be in good physical condition and have the ability to cooperate with MRI examinations - Must have underwent SWI Exclusion Criteria: - MRI contraindications present, such as cardiac pacemaker, cardiac stents, or metal implants - Head MRI or carotid artery ultrasound suggests the presence of severe stenosis or occlusion in the intracranial or extracranial segments of the cerebral arteries - Severe comorbid diseases, such as cardiac, pulmonary, hepatic, and renal insufficiencies

Study Design


Intervention

Other:
cerebral microbleeds
Whether patients with acute ischemic stroke are complicated by cerebral microbleeds

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Xin Guo

Outcome

Type Measure Description Time frame Safety issue
Primary Comparison of clinical data between AIS patients in CMB and non-CMB groups Differences in general information between AIS patients in CMB and non-CMB groups from January 2014 to December 2015
Primary Comparison of clinical data between male and female AIS patients Differences in general informationbetween male and female AIS patients from January 2014 to December 2015
Primary Comparison of CMB-related characteristics between the male and female AIS patients Differences in CMB-related characteristics between the male and female AIS patients from January 2014 to December 2015
Primary Predictive factor analysis for CMBs in male AIS patients CMB-related factors in male AIS patients from January 2014 to December 2015
Primary Predictive factor analysis for CMBs in female AIS patients CMB-related factors in female AIS patients from January 2014 to December 2015
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