Actively Recruiting
Clinical Performance and Quality Measures for Adults With Acute ST-Elevation Myocardial Infarction in China
Led by China National Center for Cardiovascular Diseases · Updated on 2019-10-09
200000
Participants Needed
1
Research Sites
911 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This study aims to investigate and evaluate clinical performance and quality measures for adults with acute ST-elevation myocardial infarction (STEMI) in China. Further more, the investigates like to develop quality improvement strategies and relevant tools focusing on treatment and clinical outcome in patients with STEMI. This is a annually survey , through consecutively recruiting all eligible inpatients and collecting relevant medical information, the performance of all participating hospitals. Further, quality improvement strategies including summary of clinical performance and quality measures, clinical pathways and team building will be organized for the purpose of quality improvement. All hospitals will consecutively recruit qualified patients in the same method adopted in baseline period. Then the reperfusion rates and other performance measures will be compared annually.
CONDITIONS
Official Title
Clinical Performance and Quality Measures for Adults With Acute ST-Elevation Myocardial Infarction in China
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients with STEMI who arrive at the hospital within 48 hours from the symptoms onset.
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Hongjian Wang
Beijing, Beijing Municipality, China, 100037
Actively Recruiting
Research Team
H
Hongjian Wang
CONTACT
K
Kefei Dou
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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