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The Evaluation and Management of Patients With Acute ChesT Pain in China

The Evaluation and Management of Patients With Acute ChesT Pain in China

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02536677
Acronym
EMPACT
Enrollment
8374
Registered
2015-09-01
Start date
2016-01-31
Completion date
2017-10-31
Last updated
2018-01-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Chest Pain, Acute Coronary Syndrome

Keywords

Acute Chest Pain, Acute Coronary Syndrome, Evaluation and Management, Decision Aid, Healthcare Utilization

Brief summary

EMPACT is the first attempt to comprehensively evaluate the current emergency care of acute chest pain from a regional representative sample in China.Findings will allow new opportunities to facilitate the clinical quality improvements and ultimately reduce the mortality and health care burden in patients with acute chest pain. It also will help to establish a regional network and database for further research and performance improvement.

Interventions

None listed

Sponsors

People's Hospital of Jinxiang County
CollaboratorUNKNOWN
People's Hospital of Chengwu
CollaboratorUNKNOWN
Traditional Chinese Medicine Hospital of Wucheng County
CollaboratorUNKNOWN
People's Hospital of Longkou City
CollaboratorUNKNOWN
People's Hospital of Gaomi City
CollaboratorUNKNOWN
Linyi People's Hospital
CollaboratorOTHER
People's Hospital of Wenshang County
CollaboratorUNKNOWN
The 2nd People's Hospital of Liaocheng City
CollaboratorUNKNOWN
People's Hospital of Shouguang City
CollaboratorUNKNOWN
Traditional Chinese Medicine Hospital of Pingyin County
CollaboratorUNKNOWN
Traditional Chinese Medicine Hospital of Laoling City
CollaboratorUNKNOWN
The 2nd People's Hospital of Dongying City
CollaboratorUNKNOWN
Affiliated Hospital of Shandong Academy of Medical Sciences
CollaboratorUNKNOWN
People's Hospital of Shizhong District, Jinan City
CollaboratorUNKNOWN
The 2nd People's Hospital of Dezhou City
CollaboratorUNKNOWN
Central Hospital of Zibo
CollaboratorOTHER
Jining Medical University
CollaboratorOTHER
People's Hospital of Mudan, Heze City
CollaboratorUNKNOWN
The 3rd People's Hospital of Jinan City
CollaboratorUNKNOWN
Qianfoshan Hospital
CollaboratorOTHER
Xinlongzhuang Colliery Hospital
CollaboratorUNKNOWN
The 2nd Traditional Chinese Medicine Hospital of Taian City
CollaboratorUNKNOWN
Qilu Hospital of Shandong University
CollaboratorOTHER
Yuguo Chen
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Eighteen years and older 2. Presenting to the ED 3. With acute chest pain or suspected ACS 4. Symptoms occurring within 24 hours 5. Informed consent from patient or next of kin

Exclusion criteria

1. Chest pain caused by trauma 2. Persisting or recurrent chest pain caused by rheumatic diseases or cancer 3. Transferred from another grade II or grade III hospital 4. Presenting to the ED again within 30 days after initial enrollment

Design outcomes

Primary

MeasureTime frameDescription
Major adverse cardiac events (MACE)30 days after presenting to the emergency departments(ED)The primary outcome was a composite of adjudicated MACEs, including death from all causes, non-fatal acute myocardial infarction (AMI), urgent revascularization, stroke, cardiac arrest, and cardiogenic shock.

Secondary

MeasureTime frame
revisiting to ED and rehospitalization30 days after presenting to the EDs

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 25, 2026