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Inflammatory Response as a Prognostic Factor of Recurrence of Atrial Fibrillation After Ablation

Assessment of Course of Inflammatory Biomarkers Concentrations After Pulmonary Veins Isolation as a Prognostic Factor of Atrial Fibrillation Treatment Effectiveness (ACtIVE-AF Study)

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02844959
Acronym
ACtIVE-AF
Enrollment
120
Registered
2016-07-26
Start date
2016-07-31
Completion date
2018-07-31
Last updated
2016-07-26

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

Conditions

Atrial Fibrillation

Keywords

Atrial Fibrillation, Biomarkers, Inflammatory Response, C-reactive protein, FGF2, MMP8, troponin I, body temperature

Brief summary

The aim of this study is to evaluate inflammatory response as a prognostic factor of atrial fibrillation recurrency after ablation. Inflammatory response will be assessed by double measurement of C-reactive protein, fibroblast growth factor 2 (FGF2), matrix metallopeptidase 8 (MMP8) and body temperature. Dynamics of change of troponin I will be measured additionally. After ablation each patient will be monitored with ECG telemonitoring system for 7 days.

Interventions

None listed

Sponsors

Medical University of Warsaw
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

* signed consent; * criteria for ablation of atrial fibrillation.

Exclusion criteria

* previous pulmonary veins isolation; * ablation other than pulmonary veins isolation during the procedure; * atrial fibrillation at the beginning of ablation procedure; * usage of 'single shot' devices.

Design outcomes

Primary

MeasureTime frame
Atrial fibrillation within the first 7 days after ablationwithin the first 7 days after ablation

Secondary

MeasureTime frame
Atrial fibrillation within 6 months after ablation6 months

Countries

Poland

Contacts

Primary ContactMichał Peller, MD
michalpeller@gmail.com694 914 962
Backup ContactKrzysztof Ozierański, MD
krzysztof.ozieranski@gmail.com509 996 947

Outcome results

None listed

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