- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04255940
2019-nCoV Outbreak and Cardiovascular Diseases
February 3, 2020 updated by: Pan-Pan Hao, Qilu Hospital of Shandong University
Impact of a Novel Coronavirus (2019-nCoV) Outbreak on Public Anxiety and Cardiovascular Disease Risk in China
Cardiovascular events occurring after 2019-nCoV outbreak in Jinan were prospectively assessed by emergency physicians.
We compared those events with events that occurred during the past 3 months and the same months of the last year.
Study Overview
Status
Unknown
Detailed Description
This survey aims to assess whether the public anxiety from a novel coronavirus (2019-nCoV) outbreak increases cardiovascular disease risk in China.
Cardiovascular events occurring after 2019-nCoV outbreak in Jinan were prospectively assessed by emergency physicians.
We compared those events with events that occurred during the past 3 months and the same months of the last year.
Study Type
Observational
Enrollment (Anticipated)
12000
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Panpan Hao, MD
- Phone Number: 86-18560086593
- Email: panda.how@sdu.edu.cn
Study Locations
-
-
Shandong
-
Binzhou, Shandong, China
- Recruiting
- Affiliated Hospital of Binzhou Medical Universty
-
Contact:
- Min Feng, MD, PhD
-
Sub-Investigator:
- Min Feng, MD, PhD
-
Heze, Shandong, China
- Recruiting
- Heze Municipal Hospital
-
Contact:
- Lujing Meng, MD
-
Sub-Investigator:
- Lujing Meng, MD
-
Jinan, Shandong, China
- Recruiting
- The Second Hospital of Shandong University
-
Contact:
- kun Wen, MD
-
Principal Investigator:
- Kun Wen, MD
-
Sub-Investigator:
- Xuexi Hao, MD
-
Jinan, Shandong, China, 250012
- Recruiting
- Shandong University Qilu Hospital
-
Contact:
- Panpan Hao, MD, PHD
- Email: panda.how@126.com
-
Sub-Investigator:
- Yanping Liu, MD
-
Jinan, Shandong, China, 250013
- Recruiting
- Jinan Central Hospital, Shandong University
-
Contact:
- Bin Li, MD
- Email: qingquan0615@163.com
-
Sub-Investigator:
- Peixin Hu, MD
-
Principal Investigator:
- Bin Li, MD, PhD
-
Jinan, Shandong, China, 250014
- Recruiting
- First Hospital Affiliated with Shandong First Medical University
-
Contact:
- Zhongwen Zhang, MD, PHD
- Phone Number: 18553104425
- Email: zhangzhongwen521@126.com
-
Jinan, Shandong, China, 250021
- Recruiting
- Shandong Provincial Hospital, Shandong University
-
Sub-Investigator:
- Xin Zhang, MD
-
Contact:
- Xin Zhang, MD
-
Jining, Shandong, China
- Recruiting
- Jining Hospital of Traditional Chinese Medicine
-
Contact:
- Zhengyan Qu, MD
-
Sub-Investigator:
- Zhengyan Qu, MD
-
Qihe, Shandong, China
- Recruiting
- Qihe People's Hospital
-
Contact:
- Jianjun Lu, MD
-
Sub-Investigator:
- Jianjun Lu, MD
-
Qingdao, Shandong, China, 266003
- Recruiting
- Affiliated Hospital of Qingdao University Medical College
-
Contact:
- Liang Shan, MD
-
Sub-Investigator:
- Liang Shan, MD
-
Weihai, Shandong, China
- Recruiting
- Weihai Municipal Hospital
-
Contact:
- Lei Cao, MD
-
Sub-Investigator:
- Lei Cao, MD
-
Zibo, Shandong, China
- Recruiting
- Central Hospital of Zibo
-
Contact:
- Bo Li, MD, PhD
-
Sub-Investigator:
- Bo Li, MD, PhD
-
-
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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Patients visiting emergency department.
Description
Inclusion Criteria:
- Patients visiting emergency department.
Exclusion Criteria:
-
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
Cohorts and Interventions
Group / Cohort |
---|
After outbreak
|
Past 3 months
|
Last year
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Cardiovascular Death
Time Frame: 3 months
|
3 months
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Major Adverse Cardiovascular Events
Time Frame: 3 months
|
3 months
|
Times From symptom onset to hospital arrival
Time Frame: 3 months
|
3 months
|
Anxiety
Time Frame: 3 months
|
3 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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 (Actual)
January 20, 2020
Primary Completion (Anticipated)
April 30, 2020
Study Completion (Anticipated)
April 30, 2020
Study Registration Dates
First Submitted
February 3, 2020
First Submitted That Met QC Criteria
February 3, 2020
First Posted (Actual)
February 5, 2020
Study Record Updates
Last Update Posted (Actual)
February 5, 2020
Last Update Submitted That Met QC Criteria
February 3, 2020
Last Verified
February 1, 2020
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2019nCoV-CVD
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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.
Clinical Trials on Cardiovascular Death; Major Adverse Cardiovascular Events
-
AstraZenecaCompletedMajor Adverse Cardiovascular and Cerebrovascular Events (MACCE)Russian Federation
-
Medstar Health Research InstituteCompletedIncidence of Major Adverse Cardiac EventsUnited States
-
Lin ZhaoRecruitingIn-stent Restenosis | Major Adverse Cardiovascular EventsChina
-
Tianjin Chest HospitalUnknownPercutaneous Coronary Intervention | Saphenous Vein Graft Disease | Major Adverse Cardiovascular Events | Virtual Histology Intravascular UltrasoundChina
-
IRCCS San RaffaeleRecruitingDifferent Cardiomyopathy and Major Cardiovascular Adverse EventsItaly
-
University Hospital HeidelbergWithdrawnMajor Adverse Cardiovascular Events | Troponin T | GRACE ScoreGermany
-
University of MonastirCompletedChest Pain | Major Adverse Cardiovascular EventsTunisia
-
University of NebraskaCompletedVentricular Dysfunction, Left | Major Adverse Cardiac EventsUnited States
-
Centre Hospitalier Universitaire, AmiensRecruitingPeripheral Artery Disease | Critical Limb Ischemia | Major Adverse Cardiovascular Events | Major Adverse Limb Events | Hemodynamic MeasureFrance
-
China National Center for Cardiovascular DiseasesNot yet recruitingStroke | Atrial Fibrillation | Major Adverse Cardiac Events | Anticoagulant Adverse Reaction