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

NCT05476250 · ClinicalTrials.gov registry record · NA

Clinical Performance of Masimo INVSENSOR00057 for Atrial Fibrillation Detection

A NA study, sponsored by Masimo Corporation.

Terminated
Registry status
NA
Development phase
120
Enrollment target

NCT05476250: Clinical Trial NA study, sponsored by Masimo Corporation.

NCT05476250 is a NA study that was terminated before completion, run by Masimo Corporation. The registered enrollment target is 120 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (91% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT05476250, a NA study, was terminated before completion, sponsored by Masimo Corporation.

TERMINATED
Registry status
NA
Development phase
120 participants
Enrollment target

Study Summary

This study is designed to validate the performance of Masimo INVSENSOR00057 in detecting atrial fibrillation. The noninvasive ECG measurements will be compared to results obtained from an FDA-cleared ECG monitor.

Primary Outcome

Specificity refers to the ability of Masimo INVSENSOR00057 to correctly identify individuals who do not have atrial fibrillation. High specificity is important in minimizing false positives.

Interventions

  • DEVICE INVSENSOR00057

Trial Details

FieldValue
Enrollment Target 120 participants
Start Date 2022-08-01
Est. Completion 2022-08-10
Phase NA
Masimo Corporation

96 total trials

Why NCT05476250 stopped before completion

NCT05476250 is an interventional study that assigns participants to a tested intervention. The registered 120 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 (91% lower).

The record links to 0 conditions, and to 1 intervention - of which INVSENSOR00057 is the first listed.

NCT05476250 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05476250 about?

NCT05476250 is a clinical study titled "Clinical Performance of Masimo INVSENSOR00057 for Atrial Fibrillation Detection". This study is designed to validate the performance of Masimo INVSENSOR00057 in detecting atrial fibrillation. The noninvasive ECG measurements will be compared to results obtained from an FDA-cleared ECG monitor.

What is the current status of trial NCT05476250?

This trial is currently terminated. It is a NA study. The enrollment target is 120 participants. The study started on 2022-08-01. Estimated completion is 2022-08-10.

What interventions are being tested in trial NCT05476250?

The interventions under investigation include: INVSENSOR00057 (DEVICE).

Who is sponsoring clinical trial NCT05476250?

This trial is sponsored by Masimo Corporation, which has 96 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05476250's enrollment target sits among peer trials

120 762nd of 2000 higher than 1,198 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

  • NCT01174108 · 120 participants · Phase 2

    Allogeneic Hematopoietic Stem Cell Transplantation for Severe Aplastic Anemia and Other Bone Marrow Failure Syndromes Using G-CSF Mobilized CD34+ Selected Hematopoietic Precursor Cells Co-Infused With a Reduced Dose of Non-Mobilized Donor T-cells

  • NCT01627301 · 120 participants · NA

    Sympathetic Overactivity in Post-traumatic Stress Disorder

  • NCT02025023 · 120 participants · Phase 3

    Local 5-Fluorouracil Injection for the Treatment of Chalazia: A Prospective, Comparative Study

  • NCT02128906 · 120 participants · Phase 2

    Radiotherapy With Cisplatin vs. Docetaxel-cetuximab in HNSCC: ERCC1 Biomarker Enrichment and Interaction Design

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 NCT05476250, the US trial registry maintained by the National Library of Medicine. NCT05476250 (mid enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.