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COMPLETED NA

ECG Belt for CRT Response

NCT03504020 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this clinical study is to compare ECG Belt Research System managed cardiac resynchronization therapy (CRT) patients and a control CRT group with respect to left ventricular (LV) remodeling.

Conditions Studied

Interventions

  • DEVICE ECG Belt Research System

Study Locations (20)

Florida

  • University of Florida Health Shands Hospital — Gainesville
  • Florida Hospital Cardiovascular Research Institute — Orlando
  • BayCare Health System — Tampa

North Carolina

  • Atrium Health's Carolina Medical Center — Charlotte
  • Duke University Medical Center — Durham
  • North Carolina Heart and Vascular — Raleigh

Connecticut

  • Hartford Hospital — Hartford
  • Yale School of Medicine — New Haven

Louisiana

  • Cardiovascular Institute of the South — Houma
  • Advanced Cardiovascular Specialists — Shreveport

Missouri

  • Saint Lukes Hospital of Kansas City — Kansas City
  • Washington University School of Medicine — St Louis

District of Columbia

  • MedStar Washington Hospital Center — Washington D.C.

Illinois

  • NorthShore University Health System — Evanston

Iowa

  • Iowa Heart Center — West Des Moines

Trial Details

FieldValue
Enrollment Target 498 participants
Start Date 2018-07-13
Est. Completion 2022-04-20
Phase NA

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03504020

The ClinicalTrials.gov registry entry for NCT03504020 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 498 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Medtronic Cardiac Rhythm and Heart Failure, 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 Heart Failure appearing as the primary indexed condition, and to 1 intervention — of which ECG Belt Research System 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: NCT03504020 reports 20 study locations spanning 13 distinct geographic areas — top geographies include Florida, North Carolina, 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 NCT03504020 about?

NCT03504020 is a clinical study titled "ECG Belt for CRT Response". The purpose of this clinical study is to compare ECG Belt Research System managed cardiac resynchronization therapy (CRT) patients and a control CRT group with respect to left ventricular (LV) remodeling.

What is the current status of trial NCT03504020?

This trial is currently completed. It is a NA study. The enrollment target is 498 participants. The study started on 2018-07-13. Estimated completion is 2022-04-20.

What conditions does trial NCT03504020 study?

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

What interventions are being tested in trial NCT03504020?

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

Who is sponsoring clinical trial NCT03504020?

This trial is sponsored by Medtronic Cardiac Rhythm and Heart Failure, 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 NCT03504020 being conducted?

This trial has 20 study locations across Connecticut, District of Columbia, Florida, Illinois, Iowa. 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