Supraventricular Tachycardia (SVT)

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Review clinical trials related to Supraventricular Tachycardia (SVT). Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Head-to-Head (H2H) Comparison of Ambulatory Cardiac ECG Monitors in Japan

The goal of this clinical trial is to compare the yield of clinically actionable arrhythmias through the end of indicated wear duration in Zio monitor and Heartnote patch ECG devices.

Participants needed: 130
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: iRhythm Technologies, Inc.Updated: Oct 13, 2026Locations: 4
Eligibility criteria

Participant is 18 years of age and older [+3]

Participant has known permanent or persistent (i.e., 100% burden) atrial fibrill... [+13]

Status: Not yet recruiting

MAGiC - Congenital Heart DIsease

The goal of this observational study is to collect real world performance and to confirm the effectiveness and safety of the MAGiC Ablation Catheter for the treatment of supraventricular tachycardia in adult patients with congenital heart disease: To estimate the rate of acute procedural success and to estimate the rate of chronic success through 6 months post procrdure. Participants will be asked to have a cardiac ablation procedure and visit their doctor at 1 week, 1 month and 6 monhs post procedure.

Participants needed: 40
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: StereotaxisUpdated: Sep 10, 2026Duration: 6 Months
Eligibility criteria

Adult (aged 18 or older at time of consent). [+3]

Atrial fibrillation is the target arrhythmia for the catheter ablation. [+16]

Status: Recruiting

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

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).

Participants needed: 100
Trial details
Age: 18-100Biological sex: AllType: ObservationalSponsor: University of IowaUpdated: Aug 21, 2026Locations: 1Duration: 1 Day
Eligibility criteria

ED encounter for acute SVT [+2]

Neurologic status precluding survey participation due to medical instability [+3]

Status: Recruiting

Adenosine vs Diltiazem for Treatment of SVT in the ED

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.

Participants needed: 20
Trial details
Phase: Phase 4Age: 18-100Biological sex: AllType: InterventionalSponsor: Anne E. ZepeskiUpdated: May 28, 2026Locations: 1
Eligibility criteria

Adult patients (18 years and older) [+1]

Receipt of IV AV-nodal blocking agents prior to study enrollment (includes adeno... [+7]