New study aims to decode biomarkers in common heart rhythm problems
NCT ID NCT07389928
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study will measure various biomarkers in 200 people with certain heart rhythm problems (ventricular tachycardia, premature ventricular contractions, and AVNRT) who are scheduled for a catheter ablation procedure. The goal is to see if these biomarkers are linked to the specific type of arrhythmia and if they can help predict outcomes. The research is purely observational and does not involve any new treatment.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could help doctors better predict which patients will benefit most from catheter ablation and improve treatment for heart rhythm disorders.
- What could go wrong
- This is an observational study that does not test a new treatment. It may not lead to immediate changes in care, and results may not apply to all patients with arrhythmias.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 200 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Apr 2026
An estimate. Start dates often move.
- Expected to finish
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Oct 2030
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients with ventricular tachycardia (VT), premature ventricular contractions (PVC), atrioventricular nodal reentrant tachycardia (AVNRT) undergoing catheter ablation.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion criteria: * Age ≥ 18 years * Catheter ablation due to VT, PVC, or AVNRT * Written informed consent Exclusion criteria: * Infection or inflammatory disease at time of sampling * Pregnancy * Inability to comply with study procedures * Life expectancy \< 1 year not due to arrhythmia
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
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Other studies related to the condition(s) this trial covers.
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