Skip to content

RAte Control Efficacy in Permanent Atrial Fibrillation

RAte Control Efficacy in Permanent Atrial Fibrillation, a Comparison Between Lenient Versus Strict Rate Control in Patients With and Without Heart Failure.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00392613
Enrollment
500
Registered
2006-10-26
Start date
2005-01-31
Completion date
Unknown
Last updated
2010-01-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Persistent Atrial Fibrillation

Brief summary

The investigators hypothesis is that in patients with permanent AF lenient rate control is not inferior to strict rate control in terms of cardiovascular mortality, morbidity, neurohormonal activation, NYHA class for heart failure, left ventricular function, left atrial size, quality of life and costs. Lenient rate control is defined as a resting heart rate \<110 bpm.Strict rate control is defined as a mean resting heart rate \< 80 beats per minute (bpm) and heart rate during minor exercise \< 110 bpm. Patients will be seen after 1, 2, 3 months (for titration of rate control drugs) and thereafter yearly.

Detailed description

Study objectives: 1. To show that lenient rate control is not inferior to strict rate control in terms of cardiovascular mortality and morbidity 2. To show that lenient rate control is not inferior to strict rate control in terms of all cause mortality, cardiovascular hospitalizations, NYHA class for exercise tolerance, left ventricular function and left atrial size, quality of life, neurohormonal activation as measured by NT-proBNP, hospitalization for heart failure, syncope, sustained ventricular tachycardia, appropriate shocks or anti-tachycardia pacing of ICD for ventricular arrhythmias, cardiac arrest, and pacemaker implantations, stroke, systemic emboli, and bleeding, unstable angina pectoris and myocardial infarction, costs and renal function

Interventions

PROCEDUREStrict versus lenient rate control

Sponsors

Netherlands Heart Foundation
CollaboratorOTHER
University Medical Center Groningen
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Patients with a current episode of permanent AF \< 12 months. * Age \</= 80 years. * Mean resting heart rate \> 80 beats per minute with or without rate control medication * Oral anticoagulation (or aspirin if no risk factors for thromboembolic complications are present).

Exclusion criteria

* Paroxysmal AF * Known contra-indications for either strict or lenient rate control (e.g. previous adverse effects on negative chronotropic drugs). * Unstable heart failure defined as NYHA IV heart failure and heart failure necessitating hospital admission \< 3 months before inclusion. * Cardiac surgery \< 3 months. * Any stroke. * Current or foreseen pacemaker and/ or cardiac resynchronization therapy. * Signs of sick sinus syndrome or AV conduction disturbances (i.e. symptomatic bradycardia or asystole \> 3 seconds or escape rate \< 40 beats per minute in awake symptom-free patients). * Untreated hyperthyroidism or \< 3 months euthyroidism. * Inability to walk or bike.

Design outcomes

Primary

MeasureTime frame
Life-threatening adverse effects of RC drugs
Cardiovascular mortality
Heart failure
Stroke
Bleeding
Syncope
Ventricular tachycardia
PM / ICD implantation
Cardiac arrest

Secondary

MeasureTime frame
All cause hospitalizations
Exercise tolerance
LV function and left atrial size
Quality of life
NT-proBNP
Costs
Renal function
All cause mortality

Countries

Netherlands

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 1, 2026