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NCT03218137 · ClinicalTrials.gov registry record · Phase 4

Use of Adenosine to Determine the Electrophysiological Mechanism of Premature Ventricular Contractions

A Phase 4 study of Premature Ventricular Contraction (PVC), sponsored by Weill Medical College of Cornell University.

Recruiting
Registry status
Phase 4
Development phase
100
Enrollment target
1
Study location

NCT03218137: Recruiting Phase 4 study of Premature Ventricular Contraction (PVC), sponsored by Weill Medical College of Cornell University.

NCT03218137 is a Phase 4 study of Premature Ventricular Contraction (PVC) that is actively recruiting participants, run by Weill Medical College of Cornell University. The registered enrollment target is 100 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (81% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03218137, a Phase 4 study of Premature Ventricular Contraction (PVC), is actively recruiting participants, sponsored by Weill Medical College of Cornell University.

RECRUITING
Registry status
Phase 4
Development phase
100 participants
Enrollment target
1
Study location

Study Summary

Unblinded, controlled, non-randomized, mechanistic study to determine whether physiological mechanisms underlying PVC are sensitive to adenosine. One hundred subjects undergoing clinically-indicated, standard-of-care cardiac electrophysiology study (EPS) procedure for PVCs will receive adenosine and/or verapamil to learn if their arrhythmias are inducible similarly to sustained ventricular tachycardia.

Primary Outcome

The metrics that will be collected will be: * Baseline frequency of premature ventricular contractions (PVCs) * Frequency of premature ventricular contractions (PVCs) during adenosine administration

Interventions

  • DRUG Adenosine

Study Locations (1)

New York

  • Weill Cornell Medicine - New York

Trial Details

FieldValue
Enrollment Target 100 participants
Start Date 2017-02-13
Est. Completion 2025-12-31
Phase Phase 4

What NCT03218137 shows while recruiting

NCT03218137 is an interventional study that assigns participants to a tested intervention. The registered 100 participants enrollment target is mid-sized for trials with a published cap, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (81% lower).

The record links to 1 condition, with Premature Ventricular Contraction (PVC) appearing as the primary indexed condition, and to 1 intervention - of which Adenosine is the first listed.

NCT03218137 reports a single indexed study location in New York.

Frequently Asked Questions

What is clinical trial NCT03218137 about?

NCT03218137 is a clinical study titled "Use of Adenosine to Determine the Electrophysiological Mechanism of Premature Ventricular Contractions". Unblinded, controlled, non-randomized, mechanistic study to determine whether physiological mechanisms underlying PVC are sensitive to adenosine. One hundred subjects undergoing clinically-indicated, standard-of-care cardiac electrophysiology study (EPS) procedure for PVCs will receive adenosine and...

What is the current status of trial NCT03218137?

This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 100 participants. The study started on 2017-02-13. Estimated completion is 2025-12-31.

What conditions does trial NCT03218137 study?

This clinical trial studies the following conditions: Premature Ventricular Contraction (PVC).

What interventions are being tested in trial NCT03218137?

The interventions under investigation include: Adenosine (DRUG).

Who is sponsoring clinical trial NCT03218137?

This trial is sponsored by Weill Medical College of Cornell University, which has 701 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03218137 being conducted?

This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Premature Ventricular Contraction (PVC)

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT03218137's enrollment target sits among peer trials

100 770th of 2000 higher than 1,149 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT03218137, the US trial registry maintained by the National Library of Medicine. NCT03218137 (mid enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.