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CompletedNCT04996901Updated Dec 20, 2021

The Chinese STEMI PPCI Registry (CSPR)

An observational study in ST-segment Elevation Myocardial Infarction (STEMI), sponsored by Renmin Hospital of Wuhan University. Completed at 1 site in China. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2021-12-20.

Sponsored by Renmin Hospital of Wuhan University · Observational

Study type
Observational
Model
Case-only
Time perspective
Retrospective
Enrollment
5,594
Ages
18 Years and older
Sex
All
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Study 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.

Read the 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.

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Conditions studied

  • ST-segment Elevation Myocardial Infarction (STEMI)
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In context

Myocardial Infarction

2,744 studies on the registry are indexed under Myocardial Infarction; 418 are open to participants now.

This study's enrollment of 5,594 is above the median of 500 across 983 observational studies indexed under Myocardial Infarction.

Browse Myocardial Infarction studies →

Lead sponsor

Renmin Hospital of Wuhan University is the lead sponsor of 83 studies on the registry; 27 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

All patients with STEMI were treated by primary percutaneous coronary intervention at 7 large centers from central China.

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

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
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Study design

Observational model
Case-only
Time perspective
Retrospective
Enrollment
5,594 participants (actual)
Patient registry
No

Groups and cohorts

  • derivation cohort

    Data from Renmin Hospital of Wuhan University, The First College of Clinical Medical Science, China Three Gorges University, The Central Hospital of Enshi Tujia And Miao Autonomous Prefecture, Xiangyang No.1 People's Hospital,and Wuhan Third Hospital will be used as a derivation cohort.

    Other: no intervention

  • validation cohort

    Data from The First Affiliated Hospital of Dalian Medical University and Jiangxi Provincial People's Hopital will be used as a derivation cohort.

    Other: no intervention

Interventions

  • Otherno intervention

    no intervention

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What researchers measure

Primary outcomes

  1. in-hospital acute de novo heart failure

    Killip class ≥II

    Time frame: in-hospital outcome, until discharge

  2. cardiogenic shock

    according to the universal definition

    Time frame: in-hospital outcome, until discharge

  3. death

    according to the universal definition

    Time frame: in-hospital outcome, until discharge

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Study locations

1 site
  • Renmin Hospital of Wuhan university
    Wuhan, Hubei 430000, China
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 20, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04996901
Lead sponsor
Renmin Hospital of Wuhan University
Collaborators
The First College of Clinical Medical Science, China Three Gorges University, The First Affiliated Hospital of Dalian Medical University, Jiangxi Provincial People's Hopital, The Central Hospital of Enshi Tujia And Miao Autonomous Prefecture, Xiangyang No.1 People's Hospital, Wuhan Third Hospital
Responsible party
Sponsor
First posted
Aug 9, 2021
Start date
May 22, 2021
Primary completion
Dec 5, 2021
Completion
Dec 5, 2021
Last update
Dec 20, 2021

Study contacts

Liwei Cheng
study director · Renmin Hospital of Wuhan University

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Dec 2021. You cannot join it, but the record below documents what was studied.

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