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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01716884
Other study ID # 2011[436]
Secondary ID
Status Recruiting
Phase N/A
First received October 26, 2012
Last updated October 26, 2012
Start date December 2011
Est. completion date June 2016

Study information

Verified date October 2012
Source Peking University First Hospital
Contact Yan Zhang, MD
Phone 8610-83575180
Email drzhy1108@163.com
Is FDA regulated No
Health authority China: Ministry of Health
Study type Observational

Clinical Trial Summary

1. Registration

2. Performing in three stages

3. Major aim: Much more and standard reperfusion therapy in STEMI patients


Recruitment information / eligibility

Status Recruiting
Enrollment 4000
Est. completion date June 2016
Est. primary completion date December 2015
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Onset of STEMI within 12h

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

Exclusion Criteria:

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
China Division of Cardiology, Peking University First Hospital Beijing

Sponsors (3)

Lead Sponsor Collaborator
Peking University First Hospital Abbott Vascular, Sanofi

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary The reperfusion ratio up to 1 day No
Secondary Door to Balloon time up to 1 day No
Secondary BMS ratio up to 1 day No
Secondary health economic evaluation up to 1 year No
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