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NCT05294445Active, not recruiting

From the Emergency Department Directly to Ablation of Atrial Fibrillation Study

From the Emergency Department Directly to Ablation of Atrial Fibrillation - Study - The "EMERGE-Cryo-Study"

Source: ClinicalTrials.gov · Last updated 20 Oct 2026

Brief summary (registry, in English)

The study is a prospective, two-arm, randomized, open-label, blinded endpoint, multi-center study to investigate the impact of first line ablation in patients presenting at the emergency room with recent-onset paroxysmal or persistent atrial fibrillation.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
350 (actual)
First submitted
4 Mar 2022
Start date
Dec 2021
Primary completion date
Nov 2026
Lead sponsor
Asklepios proresearch
NCT number
NCT05294445

What you commit to

  • Study type: Interventional
  • Participants enrolled: 350
  • From Dec 2021 to the primary completion date, Nov 2026
  • 13 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Severe mitral stenosis or regurgitation, prior mitral valve reconstruction or replacement
  • Any previous left atrial ablation
  • Ongoing continuous AAD therapy with Amiodarone at baseline

Other illness

  • History of failed continuous AAD therapy with \> 1 agent. Exceptions are Beta blocker, Verapamil or "pill in the pocket"-therapy.
  • Any condition or disease, which is contraindication for AF ablation, up to the assessment of the investigator
  • Any condition or disease, which is a contraindication for antiarrhythmic drug treatment, up to the assessment of the investigator
  • Known intra-cardiac thrombus formation under continuous oral anticoagulation (defined as intake \>4 weeks)
  • Active systemic infection

Other

  • Pers. AF \> 6 Mon (one episode)
  • LA-Diameter \> 60mm
  • Any contraindication for oral anticoagulation
  • Any untreated or uncontrolled hyperthyroidism or other reversible causes for AF like alcoholism
  • Pregnant or breastfeeding woman or woman of childbearing potential not on adequate birth control
  • Co-Existence of non PV-dependent atrial Tachycardia
  • Indication for implantation of ICD or pacemaker

Who the study is looking for

  • Documented, paroxysmal or persistent AF (longest AF episode \< 6-month duration). Any ECG documentation of AF (12 lead ECG, Holter ECG or mobile ECG monitoring) needs to be presented.
  • Recent-onset AF (≤ 1 year prior to enrolment)
  • Presenting at the emergency department or outpatient clinic within the last 2 weeks because of AF, including patients with spontaneous conversion in sinus rhythm (with prior AF documentation)
  • Age ≥ 18 years
  • Subject is able and willing to give informed consent

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (13)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Kerckhoff-Klinik GmbH
Coordinator of this site? Confirm its status
Bad NauheimGermanyUnknown status
Deutsches Herzzentrum der Charité
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BerlinGermanyUnknown status
Herzzentrum Uniklinik Köln
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CologneGermanyUnknown status
Evangelisches Krankenhaus Düsseldorf
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DüsseldorfGermanyUnknown status
Cardioangiologisches Zentrum Bethanien (CCB) am Markuskrankenhaus
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FrankfurtGermanyUnknown status
Universitätsklinikum Giessen
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GiessenGermanyUnknown status
Asklepios Klinik St. Georg
Coordinator of this site? Confirm its status
HamburgGermanyUnknown status
Universitäres Herz- und Gefäßzentrum
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HamburgGermanyUnknown status
AK Altona
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HamburgGermanyUnknown status
AK Nord
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Hamburg-NordGermanyUnknown status
Asklepios Klinik Harburg
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HarburgGermanyUnknown status
Universitätsklinikum Münster
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MünsterGermanyUnknown status
St. Josefs-Hospital Wiesbaden GmbH
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WiesbadenGermanyUnknown status

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.