Actively Recruiting

Phase 4
Age: 18Years - 100Years
All Genders
NCT06993038

Adenosine vs Diltiazem for Treatment of SVT in the ED

Led by Anne E. Zepeski · Updated on 2025-09-11

20

Participants Needed

1

Research Sites

69 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This is a small, pilot study with a primary goal of assessing patient perceptions of two medication treatments for supraventricular tachycardia in adult patients treated in the Emergency Department.

CONDITIONS

Official Title

Adenosine vs Diltiazem for Treatment of SVT in the ED

Who Can Participate

Age: 18Years - 100Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult patients 18 years and older
  • Diagnosis of acute, stable supraventricular tachycardia (SVT) in the emergency department
Not Eligible

You will not qualify if you...

  • Received intravenous AV-nodal blocking agents before study enrollment (including adenosine, non-dihydropyridine calcium channel blockers, beta-antagonists)
  • History of Wolff-Parkinson-White (WPW) syndrome
  • History of heart failure with reduced ejection fraction (LVEF ≤ 40%)
  • Severe bronchoconstrictive lung disease
  • Prior hypersensitivity to study medication
  • Previously enrolled in this pilot study
  • Pregnancy
  • Incarceration

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Iowa Health Care

Iowa City, Iowa, United States, 52242

Actively Recruiting

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Research Team

A

Anne Zepeski, PharmD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

2

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