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Trending of Respiratory Rate Using the Nellcor™ Bedside Respiratory Patient Monitoring System

NCT03593603 · View on ClinicalTrials.gov ↗

Study Summary

This is an open-label, non-randomized, prospective, descriptive study of the Nellcor™ Bedside Respiratory Patient Monitoring System using the Nellcor™ Respiration Rate parameter and Nellcor™ Adult Respiratory Sensor The study is intended to gain further information in the clinical space on the function of the Nellcor™ Respiration Rate parameter. The primary objective is to describe spot check (e.g. manual observation) of respiration rate versus cumulative automated counting (trend) of respiratory rate as measured using the Nellcor™ Bedside Respiratory Patient Monitoring System with the Nellcor™ Respiration Rate parameter.

Interventions

  • DEVICE Nellcor™ Bedside Respiratory Monitoring System

Study Locations (2)

Oklahoma

  • St. John Health System — Tulsa

Washington

  • MultiCare Institute for Research & Innovation — Tacoma

Trial Details

FieldValue
Enrollment Target 37 participants
Start Date 2018-07-11
Est. Completion 2019-05-03

Sponsor

Medtronic - MITG

89 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03593603

The ClinicalTrials.gov registry entry for NCT03593603 describes a study currently listed as completed. It is categorized as an unspecified phase, 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 37 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Medtronic - MITG, which has 89 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 Patients Prescribed Non-invasive Respiratory Monitoring appearing as the primary indexed condition, and to 1 intervention — of which Nellcor™ Bedside Respiratory Monitoring 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: NCT03593603 reports 2 study locations spanning 2 distinct geographic areas — top geographies include Oklahoma, Washington. 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 NCT03593603 about?

NCT03593603 is a clinical study titled "Trending of Respiratory Rate Using the Nellcor™ Bedside Respiratory Patient Monitoring System". This is an open-label, non-randomized, prospective, descriptive study of the Nellcor™ Bedside Respiratory Patient Monitoring System using the Nellcor™ Respiration Rate parameter and Nellcor™ Adult Respiratory Sensor The study is intended to gain further information in the clinical space on the funct...

What is the current status of trial NCT03593603?

This trial is currently completed. The enrollment target is 37 participants. The study started on 2018-07-11. Estimated completion is 2019-05-03.

What conditions does trial NCT03593603 study?

This clinical trial studies the following conditions: Patients Prescribed Non-invasive Respiratory Monitoring. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT03593603?

The interventions under investigation include: Nellcor™ Bedside Respiratory Monitoring System (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT03593603?

This trial is sponsored by Medtronic - MITG, which has 89 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT03593603 being conducted?

This trial has 2 study locations across Oklahoma, Washington. 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