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Locating heart rhythm sources in new atrial fibrillation after heart surgery

Maps heart rhythm sources in adults with new atrial fibrillation after surgery.

Plain-language title generated from the registry record
Registry title: The Basel CardioInsightTM - 3D Mapping Study

Key facts

Where
Sankt Pölten, AustriaSee the site

AI summary: who the study is looking for

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for adults who have had heart surgery and then develop a new irregular heartbeat (atrial fibrillation) within 7 days after the operation.

Age
18 years or older
Sex
All sexes can join.
Disease stage
New atrial fibrillation that starts within the first 7 days (168 hours) after cardiac surgery, in the hospital wards or intensive care at University Hospital Basel.
Earlier treatment
Must have had cardiac surgery. Must not have had left atrial ablation before, or amiodarone treatment within the last 3 months.

Main reasons for not taking part

  • Atrial fibrillation or atrial flutter documented before the surgery
  • Previous left atrial ablation or cardioembolic stroke
  • Amiodarone treatment within the last 3 months
  • Left ventricular ejection fraction below 40%
  • Mechanical circulatory support around the surgery

Read by machine on 12 November 2026.

Where in Austria

  • University Hospital St. PöltenSankt Pölten, AustriaContact: Felix Nagel, MDTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

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Trial details

Who runs it
University Hospital, Basel, Switzerland
Trial code
NCT04964765
Record updated
9 April 2025
Original description
This study is to describe the exact location of NOAF-maintaining foci and rotors after cardiac surgery identified by mapping using the non-invasive phase mapping with CardioInsightTM - 3D Mapping technology (CardioInsightTM, Medtronic Switzerland, Tolochenaz, Switzerland) and a low-dose computed tomography scan of the chest.Read full original descriptionShow less

Non-invasive Evaluation of New-onset Atrial Fibrillation After Cardiac Surgery The Basel CardioInsightTM - 3D Mapping (BigMap) Study

This study is to describe the exact location of NOAF-maintaining foci and rotors after cardiac surgery identified by mapping using the non-invasive phase mapping with CardioInsightTM - 3D Mapping technology (CardioInsightTM, Medtronic Switzerland, Tolochenaz, Switzerland) and a low-dose computed tomography scan of the chest.

Inclusion: Cardiac surgery; Signed informed consent by patient or next of kin; Mapping inclusion criteria; NOAF within the first seven postoperative days (168 hours) after cardiac surgery developing on the cardiac surgery ward, intermediate care unit or the intensive care unit of the University Hospital Basel. ICU admission will be set as starting point for observation time; General Exclusion Criteria:; Preoperative conditions:; History of previous left atrial ablation; History of cardioembolic stroke; History of amiodarone treatment within three months; Any documented history of atrial fibrillation/atrial flutter before surgery; Left ventricular ejection fraction <40%; Patient included into other study with radiation exposure; Perioperative conditions; Perioperative mechanical circulatory support (e.g., intraaortic balloon pump; extracorporeal membrane oxygenation; left ventricular assist device (e.g. Impella, Abiomed Inc., Aachen, Germany); Mapping exclusion criteria; Heart rate ≥ 50 bpm AND contraindication to adenosine; Contraindications to adenosine:; Allergy/intolerance to adenosine; History of chronic obstructive pulmonary disease (COPD Gold IV)(28); History of asthma; History of Long-QT syndrome; Hemodynamically unstable patients (margin of discretion of the attending physician).

ClinicalTrials.gov NCT04964765