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CCC Project- Acute Coronary Syndrome

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT02306616
Recruitment Status : Completed
First Posted : December 3, 2014
Last Update Posted : January 27, 2021
Sponsor:
Collaborators:
American Heart Association
Chinese Society of Cardiology
Information provided by (Responsible Party):
Dong ZHAO, Beijing Institute of Heart, Lung and Blood Vessel Diseases

Tracking Information
First Submitted Date November 29, 2014
First Posted Date December 3, 2014
Last Update Posted Date January 27, 2021
Study Start Date November 2014
Actual Primary Completion Date December 2020   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures
 (submitted: December 5, 2014)
The overall composite of 11 performance measures for ACS care [ Time Frame: Duration of hospital stay, an expected average of 1 week ]
Performance measures for ACS care including:
  1. Proportion of patients received aspirin at arrival
  2. Proportion of patients received fibrinolytic therapy within 30 mins (STEMI)
  3. Proportion of patients received primary percutaneous coronary intervention within 90 mins (STEMI)
  4. Proportion of patients received reperfusion therapy (STEMI)
  5. Proportion of patients with aspirin prescribed at discharge
  6. Proportion of patients with clopidogrel or other P2Y12 inhibitors prescribed at discharge
  7. Proportion of patients with beta-blocker prescribed at discharge
  8. Proportion of patients with statin prescribed at discharge
  9. Proportion of patients received evaluation of left ventricular systolic function
  10. Proportion of left ventricular systolic dysfunction patients with ACEI or ARB prescribed at discharge
  11. Proportion of patients received smoking cessation advice/ counseling
Original Primary Outcome Measures
 (submitted: November 29, 2014)
Performance measures for ACS care [ Time Frame: One month ]
Performance measures for ACS care including:
  1. Proportion of patients received aspirin at arrival
  2. Proportion of patients received fibrinolytic therapy within 30 mins (STEMI)
  3. Proportion of patients received primary percutaneous coronary intervention within 90 mins (STEMI)
  4. Proportion of patients received reperfusion therapy (STEMI)
  5. Proportion of patients with aspirin prescribed at discharge
  6. Proportion of patients with clopidogrel or other P2Y12 inhibitors prescribed at discharge
  7. Proportion of patients with beta-blocker prescribed at discharge
  8. Proportion of patients with statin prescribed at discharge
  9. Proportion of patients received evaluation of left ventricular systolic function
  10. Proportion of left ventricular systolic dysfunction patients with ACEI or ARB prescribed at discharge
  11. Proportion of patients received smoking cessation advice/ counseling
Change History
Current Secondary Outcome Measures Not Provided
Original Secondary Outcome Measures Not Provided
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title CCC Project- Acute Coronary Syndrome
Official Title Improving Care for Cardiovascular Disease in China: A Collaborative Project of AHA and CSC (CCC Project) - Acute Coronary Syndrome
Brief Summary To develop and implement quality improvement programs for the treatment of acute coronary syndrome (ACS) in China based on the successful experience of the AHA-Get with the Guidelines program. This program will use data collection, analysis, feedback, and process improvement to extend the use of evidence-based guidelines throughout the healthcare system and improve patient care of acute coronary syndrome.
Detailed Description Not Provided
Study Type Observational
Study Design Observational Model: Case-Only
Time Perspective: Retrospective
Target Follow-Up Duration Not Provided
Biospecimen Not Provided
Sampling Method Non-Probability Sample
Study Population Hospitalized patients with acute coronary syndrome
Condition Acute Coronary Syndrome
Intervention Not Provided
Study Groups/Cohorts Not Provided
Publications *

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status Completed
Actual Enrollment
 (submitted: January 26, 2021)
124363
Original Estimated Enrollment
 (submitted: November 29, 2014)
76500
Actual Study Completion Date December 2020
Actual Primary Completion Date December 2020   (Final data collection date for primary outcome measure)
Eligibility Criteria

Inclusion Criteria:

Hospitalized patients with discharge diagnosis as acute coronary syndrome (including STEMI, NSTEMI and UAP) in 150 tertiary and 100 secondary hospitals.

Exclusion Criteria:

None

Sex/Gender
Sexes Eligible for Study: All
Ages Child, Adult, Older Adult
Accepts Healthy Volunteers No
Contacts Contact information is only displayed when the study is recruiting subjects
Listed Location Countries China
Removed Location Countries  
 
Administrative Information
NCT Number NCT02306616
Other Study ID Numbers CCC-ACS-2014
Has Data Monitoring Committee Not Provided
U.S. FDA-regulated Product Not Provided
IPD Sharing Statement Not Provided
Current Responsible Party Dong ZHAO, Beijing Institute of Heart, Lung and Blood Vessel Diseases
Original Responsible Party Same as current
Current Study Sponsor Beijing Institute of Heart, Lung and Blood Vessel Diseases
Original Study Sponsor Same as current
Collaborators
  • American Heart Association
  • Chinese Society of Cardiology
Investigators
Principal Investigator: Dong Zhao, Ph. D Beijing Institute of Heart, Lung and Blood Vessel Diseases
PRS Account Beijing Institute of Heart, Lung and Blood Vessel Diseases
Verification Date January 2021