The SAFE Prospective Registry

Sponsor
University Hospital Ostrava (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05794464
Collaborator
(none)
60
1
1
39
1.5

Study Details

Study Description

Brief Summary

Secretoneurin (SN) is a neuropeptide from the chromogranin family that influences intracellular calcium handling. SN suppresses calcium leakage from the sarcoplasmic reticulum through the ryanodine receptor. SN is a novel biomarker that has shown the potential to predict adverse arrhythmic events.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Catheter ablation and/or electrical cardioversion
N/A

Detailed Description

The aim of the study is to sample SN before and after catheter ablation (CA) for atrial fibrillation (Afib) to predict the recurrence after CA. Also, the uric acid/albumin ratio will be assessed as a marker of Afib recurrence. Since the uric acid/albumin ratio has been shown to be predictive of Afib in patients with myocardial infarction moreover incidence of atrial fibrillation is higher in patients with gout. As a side branch marker for silent brain injury, neuron-specific enolase (NSE) and protein S100B will be evaluated. NSE showed in small trials a significant increase after catheter ablation, as well as S100B. The prognostic power is not clear yet. From the systematic review, the most powerful predictors seem to be N-terminal (NT)-prohormone B-type natriuretic peptide (NT-Pro-BNP/BNP), high-sensitivity C-reactive protein (hs-CRP), interleukin-6 (IL-6) and Carboxy-terminal telopeptide of collagen type I. Biomarkers are divided into 3 main types: congestion, inflammation, and renal function.

Patients will be enrolled before catheter ablation/electrical cardioversion for Afib after signing IS, and the blood sampling will be performed the day before and the day after catheter ablation. In the electric cardioversion arm, the blood sampling will be performed before electrical cardioversion and 2h after the cardioversion before discharge.

Patients will be followed for recurrency - all patients will have a 24-hour ECG Holter and External loop recorder (MDT) for two weeks after the three months of the blanking period. Clinical outpatient control will ensue in the 4th, eighth,12, and 24 months.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Intervention Model Description:
The study subjects will be enrolled in one group.The study subjects will be enrolled in one group.
Masking:
None (Open Label)
Masking Description:
No masking will be used in the study.
Primary Purpose:
Other
Official Title:
Secretoneurin as a Biomarker of Atrial Fibrillation rEcurrence After Catheter Ablation/Electrical Cardioversion
Anticipated Study Start Date :
May 1, 2023
Anticipated Primary Completion Date :
May 1, 2026
Anticipated Study Completion Date :
Aug 1, 2026

Arms and Interventions

Arm Intervention/Treatment
Experimental: Catheter ablation and/or electrical cardioversion

Study subjects indicated for catheter ablation and/or electrical cardioversion will be enrolled in this study arm.

Procedure: Catheter ablation and/or electrical cardioversion
Catheter ablation and/or electrical cardio version are procedures intended to treat atrial fibrillation.

Outcome Measures

Primary Outcome Measures

  1. Atrial fibrillation recurrence based on secretoneurin levels [24 months]

    Atrial fibrillation recurrence based on secretoneurin levels will be assessed

Secondary Outcome Measures

  1. Brain injury detection [24 months]

    Brain injury will be detected using serum protein S100B and neuron specific enolase.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Atrial fibrillation (Afib); (paroxysmal, persistent)

  • Patients indicated for catheter ablation and/or electrical cardioversion

  • Signed informed consent

Exclusion Criteria:
  • Longstanding or permanent atrial fibrillation

  • Severe mitral regurgitation

  • Heart failure with a permanently reduced ejection fraction

  • Cerebral ischaemic stroke in < 3 months

  • Severe kidney injury

  • Severe renal insufficiency

  • Hepatic insufficiency limiting biomarker sampling

  • Myocardial infarction < 3 months

Contacts and Locations

Locations

Site City State Country Postal Code
1 University Hospital Ostrava Ostrava Moravian-Silesian Region Czechia 70852

Sponsors and Collaborators

  • University Hospital Ostrava

Investigators

  • Principal Investigator: Jiří Plášek, MD,PhD,FESC, University Hospital Ostrava

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
University Hospital Ostrava
ClinicalTrials.gov Identifier:
NCT05794464
Other Study ID Numbers:
  • FNO-IKK-SAFE
First Posted:
Apr 3, 2023
Last Update Posted:
Apr 3, 2023
Last Verified:
Mar 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University Hospital Ostrava
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 3, 2023