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CompletedNCT01877876Updated Jun 10, 2015

Assessing the Accuracy of the RevK Sensor

An observational study in Patients Undergoing Spine Surgery, sponsored by University of California, San Francisco. Completed at 1 site in United States. Open to participants aged 18 Years to 85 Years. Per ClinicalTrials.gov, last updated 2015-06-10.

Sponsored by University of California, San Francisco · Observational

Study type
Observational
Time perspective
Prospective
Enrollment
8
Ages
18 Years to 85 Years
Sex
All
01

Study summary

Evaluation of a new generation of sensors for monitoring blood hemoglobin. The newest version is RevK.

Read the detailed description

Evaluation of a new generation of sensors for monitoring blood hemoglobin with the Masimo non-invasive hemoglobin monitor. The newest sensor version is RevK.

02

Conditions studied

  • Patients Undergoing Spine Surgery
03

In context

Lead sponsor

University of California, San Francisco is the lead sponsor of 2,132 studies on the registry; 375 are open to participants now.

Of its 262 completed or terminated interventional studies of FDA-regulated products, 196 (75%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 85 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients undergoing spine surgery

Inclusion criteria

  • Male or non-pregnant female
  • American Society of Anesthesiology Classification 1, 2 or 3
  • Scheduled to undergo spine or hip surgery

Exclusion criteria

Exclusion Criteria:

  • Pregnant or nursing
  • Patients who in the study investigators clinical judgement would not be suitable for research
05

Study design

Time perspective
Prospective
Enrollment
8 participants (actual)
Patient registry
No

Groups and cohorts

  • Patient undergoing spine surgery
06

What researchers measure

Primary outcomes

  1. To assess the accuracy of the RevK sensor for measuring blood hemoglobin compared to a laboratory-derived hemoglobin value.

    Primary outcome is based on the difference between a value from the SpHb (Masimo SpHb™ continuous hemoglobin reading) minus tHb (laboratory hemoglobin determination).

    Time frame: Intermittently during spine surgery

07

Study locations

1 site
  • University of California, San Francisco
    San Francisco, California 94143, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 10, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01877876
Lead sponsor
University of California, San Francisco
Responsible party
Sponsor
First posted
Jun 14, 2013
Start date
Jun 2013
Primary completion
Dec 2014
Completion
Jun 2015
Last update
Jun 10, 2015

Study contacts

Ronald D Miller, MD, MS
principal investigator · University of California, San Francisco

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jun 2015. You cannot join it, but the record below documents what was studied.

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