Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT01750463 · ClinicalTrials.gov registry record
Comparing Validity of Non-Invasive Hemoglobin Monitoring to Laboratory Results in Critically Ill Children
A clinical trial, sponsored by University of North Carolina, Chapel Hill.
- Completed
- Registry status
- 65
- Enrollment target
NCT01750463: Completed study, sponsored by University of North Carolina, Chapel Hill.
NCT01750463 is a clinical trial that has completed, run by University of North Carolina, Chapel Hill. The registered enrollment target is 65 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01750463 has completed, sponsored by University of North Carolina, Chapel Hill.
- COMPLETED
- Registry status
- 65 participants
- Enrollment target
Study Summary
This is a prospective study to determine the accuracy of the Masimo Pronto Non-Invasive Hemoglobin Monitor and associated Rainbow® probes in the detection of hemoglobin concentration in critically ill children.
Primary Outcome
We will obtain measurements using the Masimo Pronto device prior to the standard lab draw at the following time points: post admission to PICU, 12-48 hours. We will then perform analysis using Bland Altman methods to determine the degree of agreement. Data analysis will occur 1 year after enrollment completion.
Interventions
- OTHER Masimo Pronto Rad 7 Non-Invasive hemoglobin monitor
- OTHER Standard Laboratory Blood Draw and Hemoglobin Analysis
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 65 participants |
| Start Date | 2013-01 |
| Est. Completion | 2013-05 |
What the finished NCT01750463 record still lists
NCT01750463 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 65 participants, a relatively small participant target.
The record links to 0 conditions, and to 2 interventions - of which Masimo Pronto Rad 7 Non-Invasive hemoglobin monitor is the first listed.
NCT01750463 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01750463 about?
NCT01750463 is a clinical study titled "Comparing Validity of Non-Invasive Hemoglobin Monitoring to Laboratory Results in Critically Ill Children". This is a prospective study to determine the accuracy of the Masimo Pronto Non-Invasive Hemoglobin Monitor and associated Rainbow® probes in the detection of hemoglobin concentration in critically ill children.
What is the current status of trial NCT01750463?
This trial is currently completed. The enrollment target is 65 participants. The study started on 2013-01. Estimated completion is 2013-05.
What interventions are being tested in trial NCT01750463?
The interventions under investigation include: Masimo Pronto Rad 7 Non-Invasive hemoglobin monitor (OTHER), Standard Laboratory Blood Draw and Hemoglobin Analysis (OTHER).
Who is sponsoring clinical trial NCT01750463?
This trial is sponsored by University of North Carolina, Chapel Hill, which has 1,109 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
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
- NCT03366116 · 65 participants · Phase 1
5-aza-4'-Thio-2'-Deoxycytidine (Aza-TdC) in People With Advanced Solid Tumors
- NCT03603730 · 65 participants · NA
Vagal Nerve Stimulation for Functional Dyspepsia and Gastroparesis
- NCT03796559 · 65 participants · NA
Magseed Enabled Long-Term Localization of Axillary Lymph Nodes
- NCT03993106 · 65 participants · Phase 2
A Study of sEphB4-HSA in Kaposi Sarcoma
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