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Atrial Fibrillation clinical trials

View clinical trials related to Atrial Fibrillation.

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NCT ID: NCT05818592 Completed - Clinical trials for Atrial Fibrillation New Onset

Screening for Atrial Fibrillation With Self Pulse Monitoring

Start date: September 21, 2020
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to determine the efficacy of self-pulse monitoring in detecting atrial fibrillation (AF) in adult patients at increased risk of stroke. The main questions it aims to answer are: - Is self-screening an effective modality for diagnosis of AF? - Are there clinical differences and outcomes for patients who self-screen? Eligible participants will be randomized to either the intervention group or control group. The control group will continue with usual standard of care. Participants randomized to the intervention group will be asked to: - View an online educational video to teach them the appropriate way to manually check their pulse for irregularities. - Manually check their pulse for 30 seconds twice daily for 14 days. - Patients who screen positive for irregularities will be sent a 14-day wearable cardiac monitor to assess for underlying arrhythmias. Researchers will compare the intervention group to the control group to see if there are clinical differences and outcomes.

NCT ID: NCT05817318 Recruiting - Clinical trials for Arrhythmia Burden in Patients With Recurrent, Paroxysmal Atrial Fibrillation Despite Durable Pulmonary Vein Isolation

Renal Denervation in Patients With Recurrent Atrial Fibrillation After Successful Pulmonary Vein Isolation

REDE-AF
Start date: June 27, 2023
Phase: N/A
Study type: Interventional

The aim of this study is to investigate whether renal denervation can reduce arrhythmia burden in patients with recurrent, paroxysmal atrial fibrillation despite durable pulmonary vein isolation.

NCT ID: NCT05816733 Recruiting - Atrial Fibrillation Clinical Trials

Dapagliflozin Evaluation on Atrial Fibrillation Patients Followed Cox Maze IV Procedure

DETAIL-CMIV
Start date: September 1, 2023
Phase: Phase 4
Study type: Interventional

Atrial fibrillation (AF) is the most common arrhythmia, which leads to reduced cardiac output and promotes the occurrence of heart failure, and abnormal hemodynamic changes in the left atrium induce thrombosis, which seriously reduces the quality of life, and even leads to death. For patients who need cardiac surgery combined with the Cox-Maze IV (CMIV) surgical ablation, oral amiodarone postoperatively for three consecutive months was recommended as the preferred treatment option. However, the study found there were still 15%-35% of patients at risk of AF recurrence. Dapagliflozin, a sodium-glucose cotransporter 2 inhibitor, has been widely used for the treatment of type 2 diabetes mellitus and heart failure. Nonetheless, it remains unknown whether dapagliflozin can improve the recurrence of AF and reduces adverse cardiovascular events for patients who need CMIV ablation, and whether it can be routinely used for AF patients without diabetes or heart failure. Therefore, this study aims to explore the effect of postoperative oral dapagliflozin on the recurrence of AF after CMIV.

NCT ID: NCT05812261 Completed - Atrial Fibrillation Clinical Trials

Lesion Characteristics After Pulsed-Field Ablation in Patients With Atrial Fibrillation and a Left Common Ostium

PFALCO Remap
Start date: July 19, 2023
Phase:
Study type: Observational

This study aims to investigate the lesion characteristics after pulmonary vein isolation using pulsed-field ablation in patients with atrial fibrillation and a common of the left pulmonary veins. The main question it aims to answer is: In which percentage of the patients will pulsed field ablation result in successful isolation of the left common ostium? Nineteen patients will be prospectively included in OLVG. All patients will be treated with pulsed-field ablation (routine care). After the ablation procedure, an electro-anatomical map will be created using the ablation catheter and a mapping system. This map will display the left atrium and the lesion in detail. After the procedure, three experienced operators are asked to draw a line around the LCO in the anatomical map where they would have ablated if conventional radiofrequency ablation was used. The distance between the drawn line and the ablation lesion will be measured at three predefined points. The lesion is considered successful if the mean distance is within ±10mm at all measurement points.

NCT ID: NCT05810896 Enrolling by invitation - Atrial Fibrillation Clinical Trials

AF at Home: A Virtual Education Program for Patients With Atrial Fibrillation (AF)

Start date: April 12, 2023
Phase: N/A
Study type: Interventional

The goal of this study is to determine the effectiveness of a direct-to-patient virtual education program ("AF at Home") for adults with atrial fibrillation (AF). The main questions this study aims to answer are: 1. Will participants in the educational program have improvement in quality of life, self-monitoring, and self-management strategies after program completion? 2. Will patient level quality of AF care improve for participants in the educational program? Participants will be asked to: - Participate in six hours of virtual education sessions over three weeks via Zoom. - Complete online questionnaires before the program starts and after its completion.

NCT ID: NCT05810727 Not yet recruiting - Atrial Fibrillation Clinical Trials

Atrial Fibrillation Data Linkage Non-Interventional Study

Start date: July 31, 2024
Phase:
Study type: Observational

The purpose of this study is to understand temporal changes in clinical features and functions, and the relationship with outcomes of atrial fibrillation (AF). AF is a problem with speed or pattern that the heart beats. It is the most common type of arrythmia. The study will use data linkage of a single center patient data and national claims database in Korea. This study does not include an actual patient enrollment process.

NCT ID: NCT05809596 Recruiting - Stroke Clinical Trials

HEAL-LAA Clinical Trial

HEAL-LAA
Start date: October 3, 2023
Phase: N/A
Study type: Interventional

The primary objective of this study is to collect real-world data on WATCHMAN FLX™ Pro Left Atrial Appendage Closure (LAAC) Device in patients with non-valvular atrial fibrillation.

NCT ID: NCT05809362 Completed - Atrial Fibrillation Clinical Trials

WHOOP Abnormal Rhythm Notification

WARN
Start date: April 10, 2023
Phase:
Study type: Observational

The purpose of this protocol is to assess the sensitivity and specificity of a photoplethysmography (PPG)-based algorithm for the detection of atrial fibrillation as compared to a gold-standard assessment (wearable ECG patch) among a population of individuals with known atrial fibrillation and without known atrial fibrillation over a 7-day study period.

NCT ID: NCT05805189 Recruiting - Atrial Fibrillation Clinical Trials

Prospective Evaluation of Biophysical Parameters as Long-term Predictors of Pulmonary Vein Isolation

MERCY
Start date: February 9, 2023
Phase: N/A
Study type: Interventional

Current, worldwide assessments of the prevalence of AF estimate that 33 million people are affected by this cardiac arrhythmia. As the most common sustained atrial arrhythmia, AF has a well-established association with systemic embolic events, stroke, heart failure, and increased mortality. Current treatment guidelines and consensus statements for patients with AF suggest that most patients should be first managed with a pharmaceutical drug therapy; however, when a patient becomes drug refractory (intolerant or non-responsive), catheter ablation by PV isolation (PVI) is recommended. The aim of PVI is abolishment of all conducted electrical activity beyond the isolating lesions. The recent NICE guidelines have established that today RF point-by-point ablation is the most cost-effective treatment approach over a lifetime after failure of 1 or more anti-arrhythmic drugs5, but until now a new technology, HELIOSTAR, RF Balloon, has not been included in this cost-effectiveness analysis

NCT ID: NCT05804747 Recruiting - Atrial Fibrillation Clinical Trials

A Study to Evaluate Effectiveness and Safety of Edoxaban in Patients 80 Years of Age or Older With Nonvalvular Atrial Fibrillation

SILVERCARE_AF
Start date: February 16, 2023
Phase:
Study type: Observational

Non-valvular atrial fibrillation (NVAF) increases the risk of stroke by three- to five-fold, especially in elderly patients, creating a huge burden on medical system as well as a negative impact on patients' lives. Direct oral anticoagulants (DOACs) are recommended for patients with NVAF to prevent strokes. Real world data reveal the underuse of anticoagulation in the elderly, especially due to physicians' concern of bleeding, often neglecting the thromboembolic risk. This study is designed to evaluate the safety and effectiveness of edoxaban in Korean elderly patients with atrial fibrillation.