Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT03476187 · ClinicalTrials.gov registry record · NA

Benefits of µCor in Ambulatory Decompensated Heart Failure

A NA study, sponsored by Zoll Medical Corporation.

Completed
Registry status
NA
Development phase
257
Enrollment target

NCT03476187: Completed NA study, sponsored by Zoll Medical Corporation.

NCT03476187 is a NA study that has completed, run by Zoll Medical Corporation. The registered enrollment target is 257 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (82% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT03476187, a NA study, has completed, sponsored by Zoll Medical Corporation.

COMPLETED
Registry status
NA
Development phase
257 participants
Enrollment target

Study Summary

Subjects meeting the inclusion/exclusion criteria will wear the µCor for at least 90 days. During the study, clinic follow up will occur every 30 days. For all subjects, each scheduled clinic visit will include assessment of cardiac symptoms and any relevant clinically actionable events. The subject will be given a daily diary to track symptoms, unplanned hospital visits, medication changes, and all other heart failure related clinical events. Weekly phone calls to the subject will be given throughout the duration of the study to remind the patient to use the subject diary and to collect and record heart failure related clinical events. Subjects will be contacted six months and one year from initial enrollment to assess the vital status of the subject, any heart failure related clinical events since the end of µCor wear, and any health care utilization since the end of µCor wear.

Primary Outcome

HF Event: a hospitalization primarily due to heart failure within 90 days. Time window: The 7 days prior to the 1st heart failure hospitalization, or the final 7 days of device wear if no HF event occurred.

Interventions

  • DEVICE µCor

Trial Details

FieldValue
Enrollment Target 257 participants
Start Date 2018-08-17
Est. Completion 2024-04-09
Phase NA
Zoll Medical Corporation

24 total trials

What the finished NCT03476187 record still lists

NCT03476187 is an interventional study that assigns participants to a tested intervention. The registered 257 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (82% lower).

The record links to 0 conditions, and to 1 intervention - of which µCor is the first listed.

NCT03476187 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03476187 about?

NCT03476187 is a clinical study titled "Benefits of µCor in Ambulatory Decompensated Heart Failure". Subjects meeting the inclusion/exclusion criteria will wear the µCor for at least 90 days. During the study, clinic follow up will occur every 30 days. For all subjects, each scheduled clinic visit will include assessment of cardiac symptoms and any relevant clinically actionable events. The subject...

What is the current status of trial NCT03476187?

This trial is currently completed. It is a NA study. The enrollment target is 257 participants. The study started on 2018-08-17. Estimated completion is 2024-04-09.

What interventions are being tested in trial NCT03476187?

The interventions under investigation include: µCor (DEVICE).

Who is sponsoring clinical trial NCT03476187?

This trial is sponsored by Zoll Medical Corporation, which has 24 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03476187's enrollment target sits among peer trials

257 403rd of 2000 higher than 1,597 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT03618550 · 257 participants · Phase 2

    Phase II Study of Second- Line Pembrolizumab Plus GVD for Relapsed or Refractory Hodgkin Lymphoma

  • NCT04674267 · 257 participants · NA

    Resilience and Equity in Aging, Cancer, and Health (REACH)

  • NCT06099288 · 257 participants · NA

    Strong Families Start at Home/Familias Fuertes Comienzan en Casa

  • NCT06207084 · 257 participants · NA

    The Fit With Us Study

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT03476187, the US trial registry maintained by the National Library of Medicine. NCT03476187 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.