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COMPLETED NA

Clinical Trial Comparing Devices Used for Cardioversion of Atrial Fibrillation

NCT05992623 · View on ClinicalTrials.gov ↗

Study Summary

The goal of this single center, investigator initiated, open label prospective randomized controlled trial is to compare the efficacy of a single 200J RBW shock and a single 360J BTE shock. The secondary objective of the study is to compare the frequency of adverse events after one or two 200J RBW or 360J BTE shocks

Conditions Studied

Interventions

  • DEVICE Zoll external defibrillator
  • DEVICE Lifepak external defibrillator

Study Locations (1)

Virginia

  • Inova Health System — Falls Church

Trial Details

FieldValue
Enrollment Target 546 participants
Start Date 2023-07-21
Est. Completion 2024-12-11
Phase NA

Sponsor

Inova Health Care Services

56 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05992623

The ClinicalTrials.gov registry entry for NCT05992623 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 546 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Inova Health Care Services, which has 56 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Atrial Fibrillation appearing as the primary indexed condition, and to 2 interventions — of which Zoll external defibrillator is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT05992623 reports 1 study location spanning 1 distinct geographic area — top geographies include Virginia. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT05992623 about?

NCT05992623 is a clinical study titled "Clinical Trial Comparing Devices Used for Cardioversion of Atrial Fibrillation". The goal of this single center, investigator initiated, open label prospective randomized controlled trial is to compare the efficacy of a single 200J RBW shock and a single 360J BTE shock. The secondary objective of the study is to compare the frequency of adverse events after one or two 200J RBW o...

What is the current status of trial NCT05992623?

This trial is currently completed. It is a NA study. The enrollment target is 546 participants. The study started on 2023-07-21. Estimated completion is 2024-12-11.

What conditions does trial NCT05992623 study?

This clinical trial studies the following conditions: Atrial Fibrillation. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05992623?

The interventions under investigation include: Zoll external defibrillator (DEVICE), Lifepak external defibrillator (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05992623?

This trial is sponsored by Inova Health Care Services, which has 56 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05992623 being conducted?

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

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial