Two common heart drugs face off in race to steady a racing heart

NCT ID NCT02025465

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early This study
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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.

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 4

Runs after approval, following long-term safety and how well the treatment works in everyday use.

Participants

69 people

The number who actually took part.

Start date

Dec 2013

Finished

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

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.

Show 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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