Two common heart drugs face off in race to steady a racing heart
NCT ID NCT02025465
First seen Sep 10, 2026 · Last updated Sep 11, 2026 · Updated 1 time
Summary
Researchers compare two standard drugs, diltiazem and metoprolol, for controlling rapid heart rate in people who arrive at the emergency department with atrial fibrillation or atrial flutter. Adults with a heart rate of 100 beats per minute or higher are randomly assigned to receive one of the two drugs. The trial tracks how quickly each drug restores a normal heart rhythm, how well it controls heart rate, and whether patients can go home from the emergency department.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- diltiazem and metoprolol, two common heart-rate control drugs
- What this could lead to
- If one drug works faster or helps more patients return to a normal heart rhythm, emergency doctors could pick it first for atrial fibrillation or flutter.
- What could go wrong
- This is a small, single-center study of 69 people. The results may not apply to other hospitals or patients, and both drugs are already standard options.
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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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69 people
The number who actually took part.
- Start date
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Dec 2013
- Finished
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May 2024
- 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
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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 presenting to Charleston Area Medical Center (CAMC) General or Memorial Hospital ED with a primary diagnosis of AF/FL * Patients with a mean ventricular rate of 100 beats per minute or more within one hour of presentation Exclusion Criteria: * Under age 18 years * A diagnosis of acute coronary syndrome (ACS) made by the admitting ED physician (ST elevation myocardial infarction, non-ST elevation myocardial infarction, unstable angina) (beta blockers are a Class I medications for ACS) * Known history of heart failure with an ejection fraction \<50% * Known ejection fraction \<45%, regardless of a history of heart failure. Heart failure and a history of heart failure with an ejection fraction of 40-50% may occur with a normal ejection fraction now referred to as Heart Failure With Preserved Ejection Fraction (HFpEF) or "diastolic dysfunction". A low ejection fraction is not always associated with heart failure. Our technology of measuring ejection fraction is by no means perfect. It is acceptable to use MET in larger than usual starting doses of MET for rate control or patients with "diastolic dysfunction", but not systolic dysfunction. Thus, a patient who has an ejection fraction of 42% may possibly have an ejection fraction of 37%, possible lower. Thus the investigators want to avoid the possibility of a patient with a history of heart failure does not receive MET unless the investigators feel systolic heart failure is not present. * Systolic blood pressure \<90 mm Hg or between 90-99 AND patient is experiencing symptoms of dizziness * Known allergy or adverse reactions to diltiazem or metoprolol. This is very rare. Exclusions from ECG readings: * Current Atrioventricular (AV) block (2nd or 3rd degree) * Pre-excitation syndromes - Wolfe Parkinson White (WPW) (Accelerated AV conduction- a rare condition where MET and DT are not advised) * Pulse rate less 100/minute on ED admission (already at rate control) * Cardiogenic shock or heart failure requiring inotropic agents or intubation * Respiratory failure requiring intubation * Pregnancy or lactation (neither pregnancy or lactation are listed as definitely safe for either medication) * Asthma, defined as (asthma is a relative contraindication for MET: * current use of inhaler * use of steroids for dyspnea * history of being treated for asthma * Inability or unwillingness to provide informed consent * Physician decision * If either medication is a relative contraindication, the patient cannot be randomized.
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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
-
Charleston Area Medical Center
Charleston, West Virginia, 25304, United States
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