- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02795078
The Coexistence of Atherosclerotic Intracranial Arterial Stenosis With Intracranial Aneurysms (CAIASA)
November 3, 2017 updated by: liuxingju
To Investigate the Coexistence of Atherosclerotic Intracranial Arterial Stenosis With Intracranial Aneurysms
Atherosclerotic intracranial arterial(ICA) stenosis and intracranial aneurysms are the common causes of ischemic stroke and hemorrhagic stroke, respectively.
Investigators aimed to assess the prevalence of cerebral aneurysms in patients with atherosclerotic intracranial arterial stenosis.
Study Overview
Status
Unknown
Detailed Description
Based on prospective data of patients with symptomatic or asymptomatic ICA stenosis admitted to Beijing Tiantan Hospital between Jan 2015 and July 2016, all patients underwent brain CTA / MRA/DSA.
Investigators determined the number of the patients with intracranial aneurysms, calculated overall prevalence of the coexistence of atherosclerotic ICA stenosis with aneurysms and analyzed the clinical features.
Study Type
Observational
Enrollment (Anticipated)
700
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Beijing
-
Beijing, Beijing, China, 0086
- Recruiting
- Beijing Tiantan Hospital Capital Medical University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 80 years (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
patient who had the coexistence of intracranial Arterial Stenosis With Intracranial Aneurysms were included in this study
Description
Inclusion Criteria:
- DSA identified the coexistence of intracranial Arterial Stenosis With Intracranial Aneurysms
- Stenosis caused by atherosclerosis
Exclusion Criteria:
- patients do not agree
- Stenosis caused by no atherosclerosis disease
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
new stroke events during perioperative period
Time Frame: perioperative period
|
perioperative period
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
stroke events during follow up
Time Frame: 6 months after discharge
|
6 months after discharge
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
October 1, 2015
Primary Completion (ANTICIPATED)
December 1, 2017
Study Completion (ANTICIPATED)
March 1, 2018
Study Registration Dates
First Submitted
June 5, 2016
First Submitted That Met QC Criteria
June 8, 2016
First Posted (ESTIMATE)
June 9, 2016
Study Record Updates
Last Update Posted (ACTUAL)
November 6, 2017
Last Update Submitted That Met QC Criteria
November 3, 2017
Last Verified
November 1, 2017
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- BJTTH-001
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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