Clinical Trials Directory

Trials / Completed

CompletedNCT04513509

Rate Control in Patients With Atrial Fibrillation

The Surrogate Marker of Rate Control in Patients With Atrial Fibrillation

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
13 (actual)
Sponsor
National Taiwan University Hospital · Academic / Other
Sex
All
Age
18 Years – 90 Years
Healthy volunteers
Not accepted

Summary

To search for the best marker for the patients in atrial fibrillation with rate control

Detailed description

In an aging society, the prevalence of atrial fibrillation is increasing. The main treatment strategy is to reduce the complications of embolic stroke and heart failure. Among these patients, a group of them will choose to have "rate control" based on the heart conditions and the preference of the patients. The strategy is to control the ventricular rate by drugs to prevent the heart from failure. However, when the physicians attempt to do so, they encounter two questions: how much is the optimal drug dose? And what is the best marker we are looking to? To answer these questions, the investigators design a prospective, cross-over study to explore this issue. The participants will do cardiopulmonary exercise test (CPET) before and after treatment. They will receive another CPET if drug dose is titrated up. With the study, the investigators will understand whether a resting heart rate can be a good marker for optimal drug dosage, and what is the optimal range of heart rate the physicians should target.

Conditions

Interventions

TypeNameDescription
DRUGAtenolol, Bisoprolol, Metoprolol, Nebivolol, Propranolol, Diltiazem, Verapamil, digoxinStart with empirical lower dose for 3 months, and then titrate up

Timeline

Start date
2020-10-21
Primary completion
2022-06-21
Completion
2022-07-01
First posted
2020-08-14
Last updated
2026-01-16

Locations

1 site across 1 country: Taiwan

Source: ClinicalTrials.gov record NCT04513509. Inclusion in this directory is not an endorsement.