NCT04347330

Cardiovascular Risk Reduction in Atrial Fibrillation Trial

Beijing Anzhen Hospital·ClinicalTrials.gov·drugRecruiting
View on ClinicalTrials.gov
Study focus
Drug/Device/Intervention
Intensive BP Control
Study type
Interventional
Intervention type
drug
Sponsor & location
Primary sponsor
Beijing Anzhen Hospital
Location
Beijing, China
Timeline & enrollment
Phase
N/A
Start date
Aug 31, 2020
End date
Aug 01, 2025
Enrollment
6000 participants
Primary outcome

Composite cardiovascular outcomes

Summary

Atrial fibrillation (AF) is a serious public health problem because of its increasing
 incidence and prevalence in the aging population. AF is associated with elevated risks of
 death, stroke, coronary event, heart failure, cognitive decline, and chronic kidney disease.
 To identify preventive interventions for major cardiovascular events beyond effective
 anticoagulation should be a major priority in the treatment of AF patients. The CRAFT study
 is a 2-arm, multicenter, randomized clinical trial designed to test whether intensive blood
 pressure control will reduce the risk of major cardiovascular events in AF patients.

ICD-10 classifications
Chronic atrial fibrillationPersistent atrial fibrillationParoxysmal atrial fibrillationAtrial fibrillation and flutterAtrial fibrillation and atrial flutter, unspecified
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT04347330
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT04347330 through Pure Global AI's free database. This phase not specified trial is sponsored by Beijing Anzhen Hospital and is currently Recruiting. The study focuses on Atrial Fibrillation,Hypertension. Target enrollment is 6000 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.