Adenosine vs Diltiazem for SVT in the ED

This study is looking at two common medications, adenosine and diltiazem, to treat a fast heart rhythm called supraventricular tachycardia (SVT) in adults who come to the emergency department. The main goal is to understand how patients feel about these treatments. You might be able to join if you are 18 or older and have SVT. The study aims to enroll 20 people and is currently unclear if it's recruiting. Success for this study means understanding patient perceptions of these treatments within 24 hours of starting.

Study design
This is a small pilot study aiming to enroll 20 adult participants. It compares two interventions: adenosine and diltiazem.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Participants will be followed from enrollment until the end of their emergency department visit, up to 24 hours.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT06993038

Adenosine vs Diltiazem for Treatment of SVT in the ED

Recruiting
PHASE4Ages 18+InterventionalTreatment
Anne E. Zepeski
~20 participants
Updated 2026-05-28 on ClinicalTrials.gov
What's tested:adenosinediltiazem

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Feasibility outcome
Measured over From enrollment to the end of ED encounter (up to 24 hours).
+2 more outcomes measured
Supraventricular Tachycardia (SVT)
1 sites across 1 states
Iowa1
  • Anne Zepeski, PharmD · PRINCIPAL_INVESTIGATOR · University of Iowa

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  • Feasibility outcomeFrom enrollment to the end of ED encounter (up to 24 hours).

    Patients with stable SVT are identified in the ED (Threshold \>90%)

  • Feasibility outcomeFrom enrollment to the end of ED encounter (up to 24 hours).

    Eligible participants who provide consent to participate (Threshold \>50%)

  • Feasibility outcomeFrom enrollment to the end of ED encounter (up to 24 hours).

    Participants who complete all study procedures (Threshold \>80%)