The Evaluation and Management of Patients With Acute Chest Pain in China
2 other identifiers
observational
18,000
1 country
7
Brief Summary
The purpose of this study is to describe the characteristics, evaluation, management and outcomes of acute chest pain, and to provide opportunities for future initiatives to improve the emergency care for patients experiencing acute chest pain in China.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Oct 2014
Typical duration for all trials
7 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 1, 2014
CompletedFirst Submitted
Initial submission to the registry
February 26, 2015
CompletedFirst Posted
Study publicly available on registry
March 10, 2015
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2016
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2016
CompletedMarch 10, 2015
March 1, 2015
2.2 years
February 26, 2015
March 9, 2015
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
in-hospital mortality
During hospital stay,an expected average of 7 days
Secondary Outcomes (3)
Time between symptom onset and hospital admission
Time interval from symptom onset to arrival at the Emergency Department,an expected median of 9 hours
Major adverse cardiac events (MACE)
1 year
Cost-Effectiveness Analysis
1 year
Eligibility Criteria
consecutive patients attending the emergency department in 7 Chinese grade Ⅲ hospitals
You may qualify if:
- Acute chest pain(pain in the area inferior to the clavicle, superior to the rib arch, and anterior to the bilateral posterior axillary line);
- Possible Acute Coronary Syndrome;
- Symptoms occurring within last 24 hours;
- Informed consent from patient or next of kin.
You may not qualify if:
- Arrhythmia or heart failure not cause by myocardial ischemia;
- Confirmed lung disease without chest pain;
- No onset of symptoms within last 24 hours;
- No written consensus.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Yuguo Chenlead
- National Health and Family Planning Commission, P.R.Chinacollaborator
- West China Hospitalcollaborator
- Xinhua Hospital, Shanghai Jiao Tong University School of Medicinecollaborator
- Shanghai Chest Hospitalcollaborator
- First Affiliated Hospital of Harbin Medical Universitycollaborator
- Second Affiliated Hospital of Xi'an Jiaotong Universitycollaborator
- Henan Provincial People's Hospitalcollaborator
- Shandong Universitycollaborator
Study Sites (7)
First Affiliated Hospital of Harbin Medical University
Harbin, Heilongjiang, 150001, China
Henan Provincial Hospital
Zhengzhou, Henan, 450003, China
Second Affiliated Hospital of Xi'an Jiaotong University
Xi'an, Shaanxi, 710004, China
Qilu Hospital of Shandong University
Jinan, Shandong, 250012, China
Shanghai Chest Hospital
Shanghai, Shanghai Municipality, 200030, China
Xinhua Hospital, Shanghai Jiao Tong University School of Medicine
Shanghai, Shanghai Municipality, 200092, China
West China Hospital
Chengdu, Sichuan, 610041, China
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Yuguo Chen, M.D., Ph.D.
Qilu Hospital of Shandong University
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 1 Year
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- President-elect, Chinese Society of Emergency Medicine;Director, Chest Pain Center, Qilu Hospital of Shandong University
Study Record Dates
First Submitted
February 26, 2015
First Posted
March 10, 2015
Study Start
October 1, 2014
Primary Completion
December 1, 2016
Study Completion
December 1, 2016
Last Updated
March 10, 2015
Record last verified: 2015-03