Computer-based Online Database of Acute Stroke Patients for Stroke Management Quality Evaluation
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ClinicalTrials.gov Identifier: NCT04487340 |
Recruitment Status :
Recruiting
First Posted : July 27, 2020
Last Update Posted : November 23, 2022
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Sponsor:
Second Affiliated Hospital, School of Medicine, Zhejiang University
Collaborators:
Shaoxing People's Hospital
Affiliated Hospital of Jiaxing University
Huizhou Municipal Central Hospital
The Second Affiliated Hospital of Jiaxing University
Jinhua Center Hospital
Taizhou Hospital
Information provided by (Responsible Party):
Second Affiliated Hospital, School of Medicine, Zhejiang University
Tracking Information | |||||
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First Submitted Date | July 19, 2020 | ||||
First Posted Date | July 27, 2020 | ||||
Last Update Posted Date | November 23, 2022 | ||||
Actual Study Start Date | January 1, 2016 | ||||
Estimated Primary Completion Date | July 1, 2027 (Final data collection date for primary outcome measure) | ||||
Current Primary Outcome Measures |
Independence (mRS 0-2) at 1 year [ Time Frame: 1 year ] | ||||
Original Primary Outcome Measures | Same as current | ||||
Change History | |||||
Current Secondary Outcome Measures |
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Original Secondary Outcome Measures | Same as current | ||||
Current Other Pre-specified Outcome Measures | Not Provided | ||||
Original Other Pre-specified Outcome Measures | Not Provided | ||||
Descriptive Information | |||||
Brief Title | Computer-based Online Database of Acute Stroke Patients for Stroke Management Quality Evaluation | ||||
Official Title | Computer-based Online Database of Acute Stroke Patients for Stroke Management Quality Evaluation | ||||
Brief Summary | In the past three decades, the burden of stroke has increased in China and has gradually become the leading cause of death. The data acquisition and medical quality management still need to be improved in China. The purpose of this study was to establish online database of acute stroke patients for stroke management quality evaluation in China. | ||||
Detailed Description | This study is a prospective multi-center registration study. The data of acute ischemic stroke patients who underwent reperfusion therapy were registered on emergency platform. The data of stroke patients who were hospitalized were registered on stroke meidical quality control platform. The information including demographics, risk factors (history of hypertension, diabetes, stroke/TIA or atrial fibrillation, etc), prior antiplatelet usage, onset to door time (ODT), baseline National Institutes of Health Stroke Scale (NIHSS) score, baseline infarct core volume, laboratory data, ect were recorded. Clinical outcome at 3 months and 1 year was assessed. | ||||
Study Type | Observational [Patient Registry] | ||||
Study Design | Observational Model: Case-Only Time Perspective: Prospective |
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Target Follow-Up Duration | 5 Years | ||||
Biospecimen | Not Provided | ||||
Sampling Method | Non-Probability Sample | ||||
Study Population | All acute stroke patients who were admitted to hospital. | ||||
Condition | Stroke, Acute | ||||
Intervention | Behavioral: Education
Provide each center with relevant education of guidelines, and help the clinicians to improve medical quality.
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Study Groups/Cohorts | Not Provided | ||||
Publications * | Wang J, Zhang J, Gong X, Zhang W, Zhou Y, Lou M. Prediction of large vessel occlusion for ischaemic stroke by using the machine learning model random forests. Stroke Vasc Neurol. 2022 Apr;7(2):94-100. doi: 10.1136/svn-2021-001096. Epub 2021 Oct 26. | ||||
* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. |
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Recruitment Information | |||||
Recruitment Status | Recruiting | ||||
Estimated Enrollment |
200000 | ||||
Original Estimated Enrollment | Same as current | ||||
Estimated Study Completion Date | July 1, 2028 | ||||
Estimated Primary Completion Date | July 1, 2027 (Final data collection date for primary outcome measure) | ||||
Eligibility Criteria | Inclusion Criteria: Acute stroke patients Exclusion Criteria: No |
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Sex/Gender |
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Ages | Child, Adult, Older Adult | ||||
Accepts Healthy Volunteers | No | ||||
Contacts |
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Listed Location Countries | China | ||||
Removed Location Countries | |||||
Administrative Information | |||||
NCT Number | NCT04487340 | ||||
Other Study ID Numbers | CASE II | ||||
Has Data Monitoring Committee | Yes | ||||
U.S. FDA-regulated Product |
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IPD Sharing Statement |
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Current Responsible Party | Second Affiliated Hospital, School of Medicine, Zhejiang University | ||||
Original Responsible Party | Same as current | ||||
Current Study Sponsor | Second Affiliated Hospital, School of Medicine, Zhejiang University | ||||
Original Study Sponsor | Same as current | ||||
Collaborators |
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Investigators |
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PRS Account | Second Affiliated Hospital, School of Medicine, Zhejiang University | ||||
Verification Date | November 2022 |