Could a muscle relaxant stop deadly heart rhythms?
NCT ID NCT04134845
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether a single dose of dantrolene, a muscle relaxant, could reduce the risk of dangerous heart rhythms in 68 people with structural heart disease who were scheduled for a procedure to treat ventricular tachycardia. Participants received either dantrolene or a placebo, and researchers measured if the drug made it harder to trigger a dangerous heart rhythm. The goal was to see if dantrolene could be a new tool to control heart rhythm problems.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- dantrolene (a muscle relaxant)
- What this could lead to
- If it works, this could point toward a new way to prevent dangerous heart rhythms in people with heart disease.
- What could go wrong
- This is a small, early-phase trial with only 68 participants, so results may not apply to everyone. Dantrolene is a muscle relaxant and may cause side effects like muscle weakness or liver issues.
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
-
Phase 2/3
Runs two stages together: whether the treatment works, then large-scale confirmation.
- Participants
-
68 people
The number who actually took part.
- Started
-
Aug 2020
- Finished
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Aug 2025
- Lead sponsor
-
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
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
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: * Greater than or equal to 18 years of age * Able to give written informed consent * Referred for catheter-based VT ablation * Structural heart disease (cardiomyopathy or RV/LV scar) * Permanent pacemaker or implantable cardioverter defibrillator Exclusion Criteria: * Mechanical ventricular support (e.g. LVAD, ECMO) * NYHA class IV heart failure * LVEF \< 20% * Morbid obesity (BMI \> 40 kg/m2) * Severe renal insufficiency (GFR\<30 mL/min) * Chronic liver disease (Child Pugh class A-C) * Current use of calcium channel blockers * Neuromuscular disorder (e.g. muscular dystrophy) * Chronic obstructive pulmonary disease or restrictive lung disease requiring oxygen * Therapy or history of intubation * Pregnant or nursing * History of dysphagia
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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.
Contacts and locations
Locations
-
Vanderbilt University Medical Center
Nashville, Tennessee, 37232, United States
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