TTrialPathMatch Me to Trials
← Back to trials
RecruitingSupraventricular Tachycardia (SVT)

PERceptions of Diltiazem Versus ADEnosine for Treatment of Supraventricular Tachycardia in the Emergency Department

Eligible age

18–100 yrs

Accepts

All genders

Locations

1 state

Healthy volunteers

No

See if you qualify for this study

Answer a few quick questions about your location and health. Takes about a minute.

Check my eligibility →

About this study

Supraventricular tachycardia (SVT) is a dysrhythmia characterized rapid heart rate, typically with rapid onset. SVT accounts for over 50,000 emergency department visits per year. Of patients with regular, narrow-complex SVT, the mainstay of therapy includes adenosine and diltiazem. Adenosine is recommend by American and European guidelines as first-line therapy, however adenosine carries unique side effects that are potentially distressing to patients, including: "feeling of impending death or doom", flushing, anxiety, shortness of breath, and chest discomfort. Diltiazem does not carry this side effect profile, but has typically been reserved as second-line treatment due to side effects of low blood pressure associated with this class of medications. Diltiazem and adenosine have not been well studied head-to-head to compare safety and efficacy of their treatment for SVT. The purpose of this study is to evaluate safety and efficacy of adenosine and diltiazem for SVT in the ED (as completed through chart review of specific patient-level outcomes) and capture patient and clinician perspectives of medication satisfaction (through administration of questionnaires).

Sponsor: University of Iowa

You may qualify if…

  • 1. ED encounter for acute SVT
  • 2. Age \>/= 18 years
  • 3. Receipt of IV adenosine and/or IV diltiazem for SVT in the ED or prehospital setting

You may not qualify if…

  • 1. Neurologic status precluding survey participation due to medical instability
  • 2. Pregnant
  • 3. Incarcerated
  • 4. Non-English speaking

Where it's recruiting

Iowa

Iowa City

Source: ClinicalTrials.gov · NCT07086560 · last updated 2026-05-28