Sign in

NCT05472012Completed

Performance of Masimo INVSENSOR00057 in Detecting Atrial Fibrillation (Afib)

Source: ClinicalTrials.gov · Last updated 22 May 2025

Brief summary (registry, in English)

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.

Status (registry)
Completed
Study type
Interventional
Enrollment
139 (actual)
First submitted
21 Jul 2022
Start date
25 Jul 2022
Primary completion date
16 Dec 2023
Lead sponsor
Masimo Corporation
NCT number
NCT05472012

What you commit to

  • Study type: Interventional
  • Participants enrolled: 139
  • From 25 Jul 2022 to the primary completion date, 16 Dec 2023
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Subject is confirmed to have concurrent active arrhythmias (e.g., PVCs, bradycardia, etc.) at the time of enrollment.

Other illness

  • Subject is allergic to adhesives or ECG gel.

Other

  • Subject whose skin is not intact in or at the vicinity of the device placement site.

Who the study is looking for

  • Subject is 18 years of age or older.
  • Subject is confirmed to have active atrial fibrillation at the time of enrollment.

Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Site 1
Coordinator of this site? Confirm its status
JacksonUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.