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China STEMI Care Project Phase 2

China STEMI Care Project Phase 2

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03011879
Enrollment
18000
Registered
2017-01-05
Start date
2015-07-31
Completion date
Unknown
Last updated
2017-01-05

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

Conditions

ST-Elevation Myocardial Infarction

Brief summary

The program is to improve STEMI medical care quality in China. With the documents issued by National Health and Family Planning Commission of the People's Republic of China, the program was initialed in at least 200 primary PCI capable hospitals together with hundreds of adjacent non-primary PCI capable hospitals in 15 provinces. STEMI patients with symptom onset within 30 days will be enrolled in 3 periods. In each period with 6-month interval, 30 patients will be enrolled consecutively from each PCI-capable center initially and from non-primary PCI capable hospitals later, thus at least 18,000 STEMI patients from primary PCI capable hospitals will be enrolled and all of them will be followed up for 1 year. Key performance indicators (KPIs) in STEMI care will be collected using both national PCI online registry and a program STEMI online registry database for the purpose of improvement of medical care. Hospital KPIs rank report and problem-based resolution will be feedback to each hospital after data analysis in each period. Comparison of every two cross-sectional data (self) and within one cross-sectional (inter-hospital) data will be used to evaluate the improvement of medical quality.

Interventions

Sponsors

Chinese Medical Doctor Association
CollaboratorOTHER
Peking University First Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* STEMI patients with symptom onset within 30 days

Exclusion criteria

* None

Design outcomes

Primary

MeasureTime frameDescription
Referfusion ratio in patients with symptom onset within 12 hours12 hoursReferfusion including primary PCI and thrombolysis is the key strategy in STEMI care
Door-to-ballnoon time in patients with symptom onset within 12 hours12 hoursDoor-to-ballnoon time is the key index to evaluate treatment of primary PCI
Door-to-needle time in patients with symptom onset within 12 hours12 hoursDoor-to-needle time is the key index to evaluate treatment of thrombolysis
Hospital admission via ambulance ratio2 years
Symptom onset to arrive in hospital2 years
Bypass ED ratio in patients with symptom onset within 12 hours12 hours
Usage of both DAPT, statin, β blocker and ACEI/ARB in patients without contraindication3 yerasDAPT means dual antiplatelet therapy
In-hospital morbidity2 yeras
1-year on time follow-up ratio1 year

Countries

China

Contacts

Primary ContactYan Zhang, MD
drzhy1108@163.com8610-83575728

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026