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NCT Number: NCT06943365

Role of Anti-TREK-1 Autoantibodies in SCVF

Short-coupled ventricular fibrillation (SCVF) is a lethal, primary electrical disorder and an important cause of unexplained cardiac arrest.1 Recent work from our group suggests that a substantial proportion of SCVF cases is associated to circulating autoantibodies targeting TREK-1, a cardiac potassium channel, resulting in an abnormal gain-of-function which is the prerequisite for the SCVF phenotype.2 This proposal is a translational multicenter study to validate anti-TREK-1 autoantibodies as a diagnostic and prognostic biomarker in a large, diversified cohort of SCVF patients (Figure 1). Functional, cellular experiments in patient-derived hiPSC cardiomyocytes and Purkinje cells will be performed to explore the cell type-specific role of TREK-1 in arrhythmogenesis, while single-nuclear RNA sequencing (snRNA-seq) will allow us to establish the transcriptomic profile (Figure 1). These results will identify the cellular substrate for SCVF.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

St-Paul's Hospital - University of British Columbia, Vancouver, British Columbia, Canada

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About this study

Please refer to the uploaded study protocol

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age ≥ 18 years
  • Diagnosis of SCVF as per current criteria
  • Willingness to provide written informed consent

Exclusion criteria

  • SCVF patients < age 18

Treatment and study plan

Repeat plasma screening for the presence or absence of anti-TREK-1 autoantibodies

Other

Semiquantitative measure of circulating anti-TREK-1 autoantibodies in plasma of study participants using a peptid microarray

DPP6 risk haplotype

Genetic

Systematic genetic screening for the Dutch DPP6 risk haplotype in all study participants and correlation of results with the presence or absence of anti-TREK-1 autoantibodies

Primary outcomes

  1. Presence of anti-TREK-1 autoantibodies at three different time points

    Time frame: 12 months

    Plasma concentrations of anti-TREK-1 autoantibodies (semiquantitative measure using a peptide microarray at three predefined time points

Secondary outcomes

  1. Time-dependent variability of plasma concentrations of anti-TREK-1 autoantibodies

    Time frame: 12 months

    Repeat plasma sampling to assess the presence/absence of anti-TREK-1 autoantibodies and time-dependent variability of antibody expression

  2. Impact of anti-TREK-1 autoantibodies on disease severity

    Time frame: 12 months

    Correlation of the presence (plasma concentration) of anti-TREK-1 autoantibodies with recurrent VF, electrical storm and appropriate ICD therapies

Study contacts

Contact information is provided by the study sponsor or research team.

Marina Sanchez, PhD

CONTACT

[email protected]

+14186568711

Paule Banville, Study coordinator

CONTACT

[email protected]

+14186568711

Sponsors and collaborators

Lead sponsor

Institut universitaire de cardiologie et de pneumologie de Québec, University Laval

Other

Registry information

Official study title

Circulating Anti-TREK-1 Autoantibodies as Diagnostic and Prognostic Biomarkers in Short-Coupled Ventricular Fibrillation

Acronym: TRACK-VF

Important dates

Study start
2025
Primary completion
2027
Study completion
2028
First posted
Apr 24, 2025
Registry last updated
Jun 16, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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