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COMPLETED NA

Hospital Wearable Defibrillator Inpatient Study

NCT02122549 · View on ClinicalTrials.gov ↗

Study Summary

This study will obtain device-human interaction evaluations for the HWD1000 within the controlled environment of the hospital as well as establish that the safety profile is similar to outpatient wearable cardioverter-defibrillators use.

Conditions Studied

Interventions

  • DEVICE HWD1000

Study Locations (8)

Florida

  • — Atlantis
  • — Jupiter

California

  • — Los Angeles

Connecticut

  • — Danbury

Iowa

  • — Iowa City

Minnesota

  • — Saint Paul

Virginia

  • — Richmond

Washington

  • — Seattle

Trial Details

FieldValue
Enrollment Target 59 participants
Start Date 2014-04
Est. Completion 2015-07
Phase NA

Sponsor

Zoll Medical Corporation

7 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02122549

The ClinicalTrials.gov registry entry for NCT02122549 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 59 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Zoll Medical Corporation, which has 7 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 In-Hospital Cardiac Arrest appearing as the primary indexed condition, and to 1 intervention — of which HWD1000 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: NCT02122549 reports 8 study locations spanning 7 distinct geographic areas — top geographies include Florida, California, Connecticut. 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 NCT02122549 about?

NCT02122549 is a clinical study titled "Hospital Wearable Defibrillator Inpatient Study". This study will obtain device-human interaction evaluations for the HWD1000 within the controlled environment of the hospital as well as establish that the safety profile is similar to outpatient wearable cardioverter-defibrillators use.

What is the current status of trial NCT02122549?

This trial is currently completed. It is a NA study. The enrollment target is 59 participants. The study started on 2014-04. Estimated completion is 2015-07.

What conditions does trial NCT02122549 study?

This clinical trial studies the following conditions: In-Hospital Cardiac Arrest. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02122549?

The interventions under investigation include: HWD1000 (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02122549?

This trial is sponsored by Zoll Medical Corporation, which has 7 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02122549 being conducted?

This trial has 8 study locations across California, Connecticut, Florida, Iowa, Minnesota. 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