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The Chinese STEMI PPCI Registry (CSPR)

The Chinese ST-Segment Elevation Myocardial Infarction Primary Percutaneous Coronary Intervention Registry

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04996901
Enrollment
5594
Registered
2021-08-09
Start date
2021-05-22
Completion date
2021-12-05
Last updated
2021-12-20

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

Conditions

ST-segment Elevation Myocardial Infarction (STEMI)

Brief summary

The purpose of this study is to develop a risk score to predict the risks of in-hospital major adverse cardiac events in ST-segment elevation myocardial infarction patients treated by primary percutaneous coronary intervention.

Detailed description

The CSPR trial is an observational clinical trial to derive and validate a readily useable risk score to identify patients at high risk of in-hospital major adverse cardiac events in 5594 patients presenting with a ST-segment elevation myocardial infarction and treated by primary percutaneous coronary intervention.

Interventions

OTHERno intervention

no intervention

Sponsors

The First College of Clinical Medical Science, China Three Gorges University
CollaboratorUNKNOWN
The First Affiliated Hospital of Dalian Medical University
CollaboratorOTHER
Jiangxi Provincial People's Hopital
CollaboratorOTHER
The Central Hospital of Enshi Tujia And Miao Autonomous Prefecture
CollaboratorOTHER
Xiangyang No.1 People's Hospital
CollaboratorOTHER
Wuhan Third Hospital
CollaboratorOTHER
Renmin Hospital of Wuhan University
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

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

Inclusion criteria

1. Age≥18 2. ST-segment elevation myocardial infarction was defined according to the universal definition of myocardial infarction 3. STEMI treated by pPCI

Exclusion criteria

1. Patient with heart failure in admission 2. STEMI with symptom-onset-to-balloon time\>24h 3. pPCI was not successful or only underwent coronary angiography 4. Killip class ≥II in admission

Design outcomes

Primary

MeasureTime frameDescription
in-hospital acute de novo heart failurein-hospital outcome, until dischargeKillip class ≥II
cardiogenic shockin-hospital outcome, until dischargeaccording to the universal definition
deathin-hospital outcome, until dischargeaccording to the universal definition

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 8, 2026