- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02181374
The Diagnosis Value of Serum Marker in Stroke Associated With Nonvalvular Atrial Fibrillation. (CE)
December 30, 2015 updated by: Xijing Hospital
The Diagnosis Value of Serum Marker in Stroke Associated With Nonvalvular Atrial Fibrillation
The purpose of this study is to evaluate the diagnostic value of serum NT - proBNP in stroke associated with nonvalvular atrial fibrilltion.
Study Overview
Status
Unknown
Conditions
Detailed Description
All included in the cases in 7 days of blood samples, the detection of serum NT - proBNP.Through the single factor analysis to determine the serum NT - proBNP central source sex stroke prediction values.
Study Type
Observational
Enrollment (Anticipated)
1000
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
-
-
Shaanxi
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Xi'an, Shaanxi, China, 710032
- Recruiting
- The Department of Neurology, Xijing Hospital
-
Contact:
- Wen Jiang, MD
- Phone Number: 02984775361
- Email: jiangwen@fmmu.edu.cn
-
Principal Investigator:
- Dong Wei, MD
-
-
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 85 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
18 ≤ Age ≤ 85; meet the clinical diagnostic criteria for acute ischemic stroke; onset within 24 hours at the same time more than one hour; it was diagnosed with experiential doctor.
Description
Inclusion Criteria:
- 18 ≤ Age ≤ 85;
- Meet the clinical diagnostic criteria for acute ischemic stroke;
- onset within 7 days;
Exclusion Criteria:
- Severe systemic disease (chronic inflammation, infection, blood system diseases, cancer, kidney failure, liver failure,heart failure);
- Nearly a month history of myocardial infarction;
- pregnant;
- Serious neurological disease that the diagnosis is unclear;
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 |
Measure Description |
Time Frame |
---|---|---|
The diagnostic value of serum NT - proBNP in stroke associated with nonvalvular atrial fibrilltion
Time Frame: 34 months
|
All included in the cases in 7 days of blood samples , the detection of serum NT - proBNP.Through the single factor analysis to determine the prediction values of serum NT - proBNP in stroke associated with nonvalvular atrial fibrilltion.
|
34 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Study Director: Wen Jiang, MD, The Department of Neurology, Xijing Hospital
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
January 1, 2012
Primary Completion (Anticipated)
September 1, 2016
Study Completion (Anticipated)
September 1, 2016
Study Registration Dates
First Submitted
June 3, 2014
First Submitted That Met QC Criteria
July 1, 2014
First Posted (Estimate)
July 3, 2014
Study Record Updates
Last Update Posted (Estimate)
January 1, 2016
Last Update Submitted That Met QC Criteria
December 30, 2015
Last Verified
December 1, 2015
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Xijing-25
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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