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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02309398
Other study ID # CCC-AF-2014
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 2015
Est. completion date December 2020

Study information

Verified date January 2021
Source Beijing Institute of Heart, Lung and Blood Vessel Diseases
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to develop and implement quality improvement programs for the treatment of atrial fibrillation (AF) 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 atrial fibrillation.


Recruitment information / eligibility

Status Completed
Enrollment 67028
Est. completion date December 2020
Est. primary completion date December 2020
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Hospitalized patients with discharge diagnosis as atrial fibrillation in 150 tertiary and 100 secondary hospitals. Exclusion Criteria: None

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
China Beijing An Zhen Hospital Beijing

Sponsors (3)

Lead Sponsor Collaborator
Beijing Institute of Heart, Lung and Blood Vessel Diseases American Heart Association, Chinese Society of Cardiology

Country where clinical trial is conducted

China, 

References & Publications (1)

Hao Y, Liu J, Smith SC, Huo Y, Fonarow GC, Ge J, Liu J, Taubert KA, Morgan L, Guo Y, Zhou M, Zhao D, Ma C; CCC-AF Investigators. Rationale and design of the improving Care for Cardiovascular Disease in China (CCC) project: a national registry to improve m — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary The overall composite of six performance measures for AF care Performance measures for AF care including:
Proportion of patients received assessment of thromboembolic risk factors
Proportion of patients discharged on warfarin or other anticoagulant drug
Proportion of patients discharged on warfarin who have PT/INR follow-up planned prior to hospital discharge
Proportion of patients with left ventricular systolic dysfunction prescribed an ACEI or ARB at hospital discharge
Proportion of patients with left ventricular systolic dysfunction prescribed a beta blocker at hospital discharge
Proportion of patients with either coronary artery disease, cerebrovascular accident/transient ischemic attack, peripheral vascular disease or diabetes who were prescribed a statin at hospital discharge
Duration of hospital stay, an expected average of 1 week
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