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NCT02498470 Clinical Trial

Prospective Registry to Assess the Cath Lab Percutaneous Coronary Intervention Long-term Outcomes: a Single Center

Coronary Artery Disease Clinical Trial

— PCI-registry  

Official title:
Prospective Registry to Assess the Cath Lab Percutaneous Coronary Intervention Long-term Outcomes: a Single Center

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT02498470
Other study ID # PCI-registry
Secondary ID
Status Recruiting
Phase N/A
First received July 12, 2015
Last updated April 12, 2016
Start date January 2008
Est. completion date December 2017

Study information
Verified date April 2016
Source Sun Yat-sen University
Contact xiaodong zhuang, MD,PhD
Phone +8602087332200
Email zxd_medicine@163.com
Is FDA regulated No
Health authority China: Health and Family Planning Commission of Changzhou
Study type Observational [Patient Registry]

Clinical Trial Summary

The registry study is to obtain the state of the percutaneous coronary intervention state treatment for coronary heart disease in the center of the first hospital of sun yat-sen unversity in a real world.

Description:

The registry study is to obtain the long-term outcomes of the percutaneous coronary intervention state treatment for coronary heart disease patients in the center of the first hospital of sun yat-sen unversity in a real world. The data are collected using an uploading system through internet.

Recruitment information / eligibility
Status Recruiting
Enrollment 10000
Est. completion date December 2017
Est. primary completion date December 2017
Accepts healthy volunteers No
Gender Both
Age group 20 Years to 90 Years
Eligibility Inclusion Criteria:

- Patients receiving coronal artery angiography or percutaneous coronary intervention therapy

Exclusion Criteria:

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Intervention

Procedure:
• percutaneous coronary intervention
All the patients receiving coronal artery angiography or percutaneous coronary intervention therapy by standard protocol

Locations
Country Name City State
China Xiaodong Zhaung Guangzhou Guangdong

Sponsors (1)
Lead Sponsor Collaborator
Xiao-dong Zhuang

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary Composite Major Adverse Cardiac Events (MACE) All death All death, myocardial infarction, revascularization 5 years No
Secondary Target Lesion Failure composite target lesion failure (TLF) defined as a composite of cardiac death, non-fatal myocardial infarction (MI) not clearly attributable to a nontarget vessel, or target lesion revascularization (TLR) (percutaneous or by coronary artery bypass grafting) 5 year No
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