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Atrial Fibrillation and Diabetes Mellitus

Impact of Individual Atrial Arrhythmia Substrate on the Outcome Following Radiofrequency-Guided Catheter Ablation for Atrial Fibrillation in Patients With Diabetes Mellitus

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05873920
Enrollment
50
Registered
2023-05-24
Start date
2023-05-09
Completion date
2025-05-31
Last updated
2023-05-24

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

Conditions

Arrhythmias, Cardiac, Atrial Fibrillation, Cardiovascular Diseases, Heart Diseases, Pathologic Processes

Brief summary

Single center prospective study to analyze the impact of diabetes mellitus on patients' outcome following radiofrequency-guided catheter ablation for atrial fibrillation.

Detailed description

A total number of 50 patients with diabetes mellitus will undergo radiofrequency-guided catheter ablation for atrial fibrillation. Pre-procedural cardiac MRI will be performed with late-gadolinium enhancement to visualize the individual amount and distribution of fibrosis in the right and left atrium. The relationship between diabetes mellitus and individual atrial arrhythmia substrates as well as patients' outcome following catheter ablation will be analyzed.

Interventions

None listed

Sponsors

Heart and Diabetes Center North-Rhine Westfalia
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients undergoing their 1st radiofrequency-guided catheter ablation for atrial fibrillation * Diabetes mellitus * Able to understand and willing to sign the Informed Consent Form. * Age ≥18 years.

Exclusion criteria

* Contraindication for DE-MRI with a full dose of gadolinium-based contrast agent. * Previous left atrial ablation or surgical procedure * Women currently pregnant, breastfeeding, or of childbearing age not currently taking or not willing to use a reliable form of contraception * Mental or physical inability to take part in the study * Morbid obesity (BMI \> 35), or inability to be placed in MRI due to body mass.

Design outcomes

Primary

MeasureTime frameDescription
atrial fibrillation recurrence12 monthsatrial fibrillation recurrence following catheter ablation

Countries

Germany

Contacts

Primary ContactDenise Guckel, MD
dguckel@hdz-nrw.de49 5731 971258
Backup ContactAstrid Kleemeyer
akleemeyer@hdz-nrw.de49 5731 971258

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026