A Study of Agreement Between Oxygen Saturation Measured by Two Probes in Infants on the Neonatal Unit - Trial NCT05065229
Access comprehensive clinical trial information for NCT05065229 through Pure Global AI's free database. This phase not specified trial is sponsored by University of Nottingham and is currently Recruiting. The study focuses on Neonatal Disease. Target enrollment is 20 participants.
This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.
Study Focus
Sponsor & Location
University of Nottingham
Timeline & Enrollment
N/A
Jul 15, 2021
Jul 15, 2022
Primary Outcome
oxygen saturation of babies using Minday 520 N and Minday 521 N
Summary
On the neonatal unit in Derby, two types of probes are in routine use: Mindray 520 N and
 Mindray 521 N. Feedback from parents and staff show that there are concerns that the two
 probes given very different oxygen saturation readings and, often, do not agree with each
 other. This has raised concerns that infants' clinical care may be affected by the choice of
 probe. It is important to know if the two probes give similar results or not to ensure that
 infants get the appropriate monitoring and respiratory support as needed for good neonatal
 care. In this study, we will compare the reading made by the two probes and determine whether
 the readings of the two probes agree with each other and if any disagreement is such that
 clinical decision making is affected by the difference.
ICD-10 Classifications
Data Source
ClinicalTrials.gov
NCT05065229
Device Trial

