RecruitingNot ApplicableNCT04612335

Device-based Rate Versus Rhythm Control in Symptomatic Recent-onset Atrial Fibrillation (RACE 9 OBSERVE-AF)

Device-based Rate Versus Rhythm Control Treatment in Patients With Symptomatic Recent-onset Atrial Fibrillation in the Emergency Department (RACE 9 OBSERVE-AF)


Sponsor

Maastricht University Medical Center

Enrollment

490 participants

Start Date

Nov 16, 2020

Study Type

INTERVENTIONAL

Conditions

Summary

Continuous heart rhythm monitoring elucidated the recurrent and transient nature of recent-onset atrial fibrillation (AF). The RACE7 ACWAS showed that a wait-and-see approach (WAS) in patients with recent-onset AF (rate control for symptom relief followed by delayed cardioversion if needed \<48h) allows spontaneous conversion to sinus rhythm in 69% of patients, obviating active cardioversion. Recurrences within one month were seen in 30% of patients in both groups, i.e. the initially chosen strategy did not affect the recurrence pattern. Considering the latter, it remains unclear whether cardioversion is needed at all, especially since cardioversion strategy does not seem to affect behaviour of the arrhythmia over time. Instead of cardioversion a watchful-waiting rate control strategy may be appropriate as initial strategy. This allows observing the electrical and clinical behavior of arrhythmia, providing a solid basis for comprehensive and effective early rhythm control. This study is a multi-center clinical randomized controlled trial to show non-inferiority of watchful-waiting with rate control versus routine care in terms of prevalence of sinus rhythm at 4 weeks follow-up, using a novel telemonitoring infrastructure to guide rate control during follow-up.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study (called RACE 9 OBSERVE-AF) is comparing two approaches to managing a recent episode of atrial fibrillation (irregular heartbeat): one that focuses on controlling heart rate, and another that aims to restore normal rhythm. It uses wearable heart monitors to track outcomes at home. **You may be eligible if...** - You have atrial fibrillation confirmed by an ECG - Your current episode of atrial fibrillation started less than 36 hours ago - You are experiencing symptoms from the irregular heartbeat - You are 18 or older and able to use a telemetric heart rhythm recorder **You may NOT be eligible if...** - You have a history of persistent atrial fibrillation (episodes lasting more than 48 hours requiring cardioversion) - You have dangerously high heart rate (over 170 bpm) or low blood pressure - You are having an acute heart attack or are in acute heart failure - You have unexplained fainting or untreated heart conduction problems (Sick Sinus Syndrome or Wolff-Parkinson-White syndrome) - You are currently enrolled in another clinical trial Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

OTHERRate control

Rate control drugs are administered to obtain symptom relief and a heart rate of \<110 bpm, followed by a 4-week telemonitoring period.

OTHERPharmacological or electrical cardioversion

Pharmacological or electrical cardioversion is performed to achieve restoration of sinus rhythm, either acutely or in a wait-and-see approach, all within 48 hours, and followed by a 4-week telemonitoring period.


Locations(14)

Vrije Universiteit Medisch Centrum

Amsterdam, Netherlands

Maastricht University Medical Center

Maastricht, Limburg, Netherlands

Noordwest Ziekenhuisgroep

Alkmaar, North Holland, Netherlands

Rijnstate

Arnhem, Netherlands

Medisch Spectrum Twente

Enschede, Netherlands

Martini Ziekenhuis

Groningen, Netherlands

Universitair Medisch Centrum Groningen

Groningen, Netherlands

Zuyderland Medisch Centrum

Heerlen, Netherlands

Alrijne Ziekenhuis

Leiderdorp, Netherlands

St Antonius Ziekenhuis

Nieuwegein, Netherlands

Radboud UMC

Nijmegen, Netherlands

Antonius Ziekenhuis

Sneek, Netherlands

St. Elisabeth TweeSteden Ziekenhuis

Tilburg, Netherlands

VieCuri Medical Centre

Venlo, Netherlands

View Full Details on ClinicalTrials.gov

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NCT04612335


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