Follow Up of patients by use of implantable loop recorders after catheter ablation of atrial flutter

Follow Up of patients by use of implantable loop recorders after catheter ablation of atrial flutter - FLUTFIB

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00009786

Enrollment

100

Registered

2018-04-12

Start date

2015-10-22

Completion date

Unknown

Last updated

2026-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

I48.9

Interventions

Group 1: During a time period of two years after catheter Ablation of atrial flutter the patients are controlled. At the time of 3, 6, 12, 18, 24 month after intervention. Documented are pre-existing

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: - age over 18 - give consent - informed consent in wirting - Ablation of typical atrial flutter

Exclusion criteria

Exclusion criteria: - age under 18 - documented atrial fibrillation

Design outcomes

Primary

Measure	Time frame
The follow-up visits be made after 3, 6, 12, 18 and 24 months. The follow ups should show how often and in which time period atrial fibrillation occur after the catheter Ablation of atrial flutter and if there are some risk factors.	—

Secondary

Measure	Time frame
- time between intervention and atrial fibrillation - appearance of other arrhythmia - use of oral anticoagulants - correlation with symptoms - identification of risk factors	—

Countries

Germany

Contacts

Public ContactMartin Huemer

Medizinische Klinik für Kardiologie der Charité-Universitätsmedizin Berlin (Campus Benjamin Franklin und Campus Virchow Klinikum)

martin.huemer@charite.de030-450513747

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Apr 4, 2026