Nerve block injection may tame deadly heart storms
NCT ID NCT07211347
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests a procedure called a stellate ganglion block, where a numbing medicine is injected near nerves in the neck to calm severe, repeated episodes of dangerous heart rhythms (electrical storm). The trial will involve 64 adults with heart disease who have not responded to standard treatments. Half will receive the injection, and the other half will not, to see if it reduces life-threatening heart events by at least 50% within 12 hours.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- stellate ganglion block (lidocaine and bupivacaine injection)
- What this could lead to
- If it works, this could provide a new, less invasive way to control life-threatening heart rhythm emergencies when standard treatments fail.
- What could go wrong
- This is a small, early-phase trial with only 64 participants, so results may not apply to everyone. The procedure carries risks like bleeding or nerve damage, and it may not reduce arrhythmias as hoped.
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.
- Phase
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Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
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About 64 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jun 2025
- Expected to finish
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Dec 2028
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.
- 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.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patients over 18 years old with structural heart disease and a diagnosis of refractory electrical storm, or those who require discontinuation of antiarrhythmics due to adverse events or contraindications to standard therapy. Exclusion Criteria: * Patients under 18 * History of heart transplant or prior cardiac denervation surgery * Anatomical contraindications for the procedure (prior neck surgery, burns, large scars, or thyroid goiter). * Genetically related polymorphic VT * End-stage renal disease on dialysis
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Genom att skicka in godkänner du våra Användarvillkor
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 places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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.
Contacts and locations
Locations
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Clinical Research Center of the Heart Institute - University of São Paulo
RECRUITINGSão Paulo, São Paulo, 05409011, Brazil
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