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

NCT01762722 · ClinicalTrials.gov registry record · NA

Nonin 4 Wavelength Cerebral Oximeter Study

A NA study, sponsored by Duke University.

Completed
Registry status
NA
Development phase
23
Enrollment target

NCT01762722: Completed NA study, sponsored by Duke University.

NCT01762722 is a NA study that has completed, run by Duke University. The registered enrollment target is 23 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01762722, a NA study, has completed, sponsored by Duke University.

COMPLETED
Registry status
NA
Development phase
23 participants
Enrollment target

Study Summary

A cerebral oximeter is a device that uses light to measure the amount of oxygen within the brain. It is similar to the device that measures the level of oxygen in the tip of the finger, known as a pulse oximeter. The cerebral oximeter consists of a sensor placed on the forehead that both emits and detects the amount of light absorbed. This study will determine how accurate the device is by comparing the displayed value on the monitor with blood samples taken simultaneously from the arterial blood in the wrist and venous blood in the neck. In order to test the device over a suitable range, the level of oxygen within the blood will be reduced in a controlled manner by reduction of the inspired oxygen concentration. This is the equivalent of ascending to an altitude of 16,000 feet. The study will be conducted in healthy volunteers.

Primary Outcome

A scatterplot is created with the forehead sensor saturation on the y-axis and the measured blood saturation on the x-axis. The line of identity is drawn representing the ideal points, meaning that the forehead sensor saturation is always the same as the blood saturation. The dispersion of the actual data points around this line of identity can be measured using a statistical calculation called Arithmetic Root Mean Square or ARMS. The smaller the ARMS the closer the data points lie around the li

Interventions

  • DEVICE Reduction of inspired oxygen

Trial Details

FieldValue
Enrollment Target 23 participants
Start Date 2009-09
Est. Completion 2012-04
Phase NA
Duke University

1,725 total trials

What the finished NCT01762722 record still lists

NCT01762722 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 23 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

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

NCT01762722 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01762722 about?

NCT01762722 is a clinical study titled "Nonin 4 Wavelength Cerebral Oximeter Study". A cerebral oximeter is a device that uses light to measure the amount of oxygen within the brain. It is similar to the device that measures the level of oxygen in the tip of the finger, known as a pulse oximeter. The cerebral oximeter consists of a sensor placed on the forehead that both emits and d...

What is the current status of trial NCT01762722?

This trial is currently completed. It is a NA study. The enrollment target is 23 participants. The study started on 2009-09. Estimated completion is 2012-04.

What interventions are being tested in trial NCT01762722?

The interventions under investigation include: Reduction of inspired oxygen (DEVICE).

Who is sponsoring clinical trial NCT01762722?

This trial is sponsored by Duke University, which has 1,725 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01762722's enrollment target sits among peer trials

23 1755th of 2000 higher than 245 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

  • NCT03616041 · 23 participants

    Capsule Endoscopy for Severe Hematochezia

  • NCT04348747 · 23 participants · Phase 2

    Dendritic Cell Vaccines Against Her2/Her3 and Pembrolizumab for the Treatment of Brain Metastasis From Triple Negative Breast Cancer or HER2+ Breast Cancer

  • NCT04587687 · 23 participants · Phase 2

    Brentuximab Vedotin and Bendamustine for the Treatment of Relapsed or Refractory Follicular Lymphoma

  • NCT04715022 · 23 participants · Phase 1

    Sympathetic-vascular Dysfunction in Obesity and Insulin Resistance (Vitamin C Study)

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT01762722, the US trial registry maintained by the National Library of Medicine. NCT01762722 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.