CClinicalTrials.gg
Status unknownNCT01716884Updated Oct 30, 2012

China STEMI-PCI Program

An observational study in ST Segment Elevation Myocardial Infarction, sponsored by Peking University First Hospital. Status unknown at 1 site in China. Per ClinicalTrials.gov, last updated 2012-10-30.

Sponsored by Peking University First Hospital · Observational

The sponsor has not verified this record recently (last verified Oct 2012), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
4,000
Sex
All
01

Study summary

  1. Registration
  2. Performing in three stages
  3. Major aim: Much more and standard reperfusion therapy in STEMI patients
02

Conditions studied

  • ST Segment Elevation Myocardial Infarction

Keywords

  • STEMI
  • reperfution
  • primary PCI
03

In context

Myocardial Infarction

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

This study's planned enrollment of 4,000 is above the median of 500 across 983 observational studies indexed under Myocardial Infarction.

Browse Myocardial Infarction studies →

Lead sponsor

Peking University First Hospital is the lead sponsor of 378 studies on the registry; 178 are open to participants now.

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

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

STEMI Patients enrolled and followed up 1 year

Inclusion criteria

  • Onset of STEMI within 12h
  • Onset of STEMI within 12-36h needing primary PCI

Exclusion criteria

Exclusion Criteria:

-

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
4,000 participants (estimated)
06

What researchers measure

Primary outcomes

  1. The reperfusion ratio

    Time frame: up to 1 day

Secondary outcomes

  1. Door to Balloon time

    Time frame: up to 1 day

  2. BMS ratio

    Time frame: up to 1 day

  3. health economic evaluation

    Time frame: up to 1 year

07

Study locations

1 of 1 sites recruiting
  • Division of Cardiology, Peking University First Hospital
    Beijing, 100034, China
    • Yong Huo, MD · Principal investigator
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 30, 2012, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01716884
Lead sponsor
Peking University First Hospital
Collaborators
Abbott Medical Devices, Sanofi
Responsible party
Yong Huo (Director of cardiovascular department, Peking University First Hospital) — Principal investigator
First posted
Oct 30, 2012
Start date
Dec 2011
Primary completion
Dec 2015 (estimated)
Completion
Jun 2016 (estimated)
Last update
Oct 30, 2012

Study contacts

Yan Zhang, MD
Contact
drzhy1108@163.com
8610-83575180

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Oct 2012. You cannot join it, but the record below documents what was studied.

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