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A Study of Agreement Between Oxygen Saturation Measured by Two Probes in Infants on the Neonatal Unit (Ag-OS)

Primary Purpose

Neonatal Disease

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Oxygen saturation probe Mindray 520 N and Mindray 521 N
Sponsored by
University of Nottingham
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Neonatal Disease

Eligibility Criteria

32 Weeks - 60 Weeks (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Infants who need oxygen saturation monitoring for clinical care
  • Infants born preterm (<37 weeks' gestation) who are < 7 days of age and need respiratory support including supplemental oxygen
  • Infants born preterm (<37 weeks' gestation) who are in supplemental oxygen at >34 weeks' gestation
  • Infants born at term gestation (< 37 weeks' gestation) who require respiratory support including supplemental oxygen
  • Infants with suspected cardiac disease

Exclusion Criteria:

  • Infants who have intravenous or arterial lines attached to either foot.
  • Infants who have any condition that may cause differential oxygen saturation or blood flow to the lower limbs such as venous thrombosis.
  • Infants who have local infections or skin lesions on either foot.
  • Infants older than 5 months of age

Sites / Locations

  • University Hospitals of Derby and Burton

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

A

B

Arm Description

Right foot no.520 Left foot no.521

Right foot no.521 Left foot no.520

Outcomes

Primary Outcome Measures

oxygen saturation of babies using Minday 520 N and Minday 521 N
Oxygen saturation readings using Minday 520 N and Minday 521 N probes simultaneously

Secondary Outcome Measures

clinical decision making
clinical decisions made, such as giving supplemental oxygen to infants on the neonatal unit following oxygen saturation readings from Minday 520 N and Mindray 521 N

Full Information

First Posted
August 4, 2021
Last Updated
September 7, 2023
Sponsor
University of Nottingham
Collaborators
University Hospitals of Derby and Burton NHS Foundation Trust
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1. Study Identification

Unique Protocol Identification Number
NCT05065229
Brief Title
A Study of Agreement Between Oxygen Saturation Measured by Two Probes in Infants on the Neonatal Unit
Acronym
Ag-OS
Official Title
A Study of Agreement Between Oxygen Saturation Measured by Two Probes in Infants on the Neonatal Unit
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Completed
Study Start Date
July 15, 2021 (Actual)
Primary Completion Date
January 11, 2023 (Actual)
Study Completion Date
January 14, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Nottingham
Collaborators
University Hospitals of Derby and Burton NHS Foundation Trust

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief 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.
Detailed Description
Continuous monitoring of oxygen saturation level is a key component of neonatal intensive care and NICE recommends that all neonatal services "ensure that systems are in place for preterm babies to have a target saturation level of 91% to 95%" and that this is monitored using "continuous pulse oximetry" (NICE Quality statement 4 in Quality Standard QS193: https://www.nice.org.uk/guidance/qs193/chapter/Quality-statement-4-Oxygen-saturation). Oxygen saturation monitoring is used to provide optimal respiratory support to preterm infants to ensure adequate oxygenation of tissues while preventing risks of conditions such as retinopathy of prematurity and bronchopulmonary dysplasia [1]. It is equally important in term born infants who require intensive care such as for determining adequate oxygenation for respiratory support and screening for congenital heart disease [2]. For these reasons, most infants in neonatal units are continuously monitored using pulse oximetry, a simple and painless test that measures blood oxygen levels by passing a small beam of light through the infant's hand or foot. This measures the changes in light absorption to calculate the levels of oxygenated and deoxygenated blood. To do this the light (or probe) has to be attached to the infant's hand or foot using a tie or a sticker. The probe must be attached firmly for the saturation monitor to pick up the correct readings. As neonatal skin is delicate and it is often difficult to stick objects to it, neonatal oxygen saturation probes are carefully designed. Many different types of saturation probes are in routine use in neonatal units. It is important to ensure that they give accurate and comparable readings. In 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Neonatal Disease

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Parallel group, randomised study
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
A computer-generated random number sequence will be obtained to determine which probe is attached to which foot. The sequence will be kept in opaque, sequentially numbered envelopes that will be opened just before the probes are attached to the feet of the participant. The clinical team nurse who will record the oxygen saturation readings will be blinded to which probe is attached to which foot by covering the feet securely after the probes have been attached. The probes will be designated as A and B. The study statistician will be blind to which probe is A and which is B until all data analyses are completed.
Allocation
Randomized
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Arm Title
A
Arm Type
Experimental
Arm Description
Right foot no.520 Left foot no.521
Arm Title
B
Arm Type
Experimental
Arm Description
Right foot no.521 Left foot no.520
Intervention Type
Device
Intervention Name(s)
Oxygen saturation probe Mindray 520 N and Mindray 521 N
Intervention Description
Two oxygen saturation probes will be used in this study: Mindray 520 N is a disposable oxygen saturation sensor for neonates and adults. It is a disposable, single-use sensor that is wrapped around the infant's arm or foot. Its ends stick together giving a firm, close contact with the skin. Mindray 521 N is another disposable oxygen saturation sensor for neonates and adults that is used on the neonatal unit in routine practice. As Mindray 520 N and 521 N are CE marked and used within their intended purposes we do not require a letter of no objection from the MHRA for that usage. The Mindray probes will be used without modification and there are no safety issues to the patient. Therefore, a letter of no objection from the MHRA is not required and this is not a medical device study under the Medical Devices Directive.
Primary Outcome Measure Information:
Title
oxygen saturation of babies using Minday 520 N and Minday 521 N
Description
Oxygen saturation readings using Minday 520 N and Minday 521 N probes simultaneously
Time Frame
12 months
Secondary Outcome Measure Information:
Title
clinical decision making
Description
clinical decisions made, such as giving supplemental oxygen to infants on the neonatal unit following oxygen saturation readings from Minday 520 N and Mindray 521 N
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
32 Weeks
Maximum Age & Unit of Time
60 Weeks
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Infants who need oxygen saturation monitoring for clinical care Infants born preterm (<37 weeks' gestation) who are < 7 days of age and need respiratory support including supplemental oxygen Infants born preterm (<37 weeks' gestation) who are in supplemental oxygen at >34 weeks' gestation Infants born at term gestation (< 37 weeks' gestation) who require respiratory support including supplemental oxygen Infants with suspected cardiac disease Exclusion Criteria: Infants who have intravenous or arterial lines attached to either foot. Infants who have any condition that may cause differential oxygen saturation or blood flow to the lower limbs such as venous thrombosis. Infants who have local infections or skin lesions on either foot. Infants older than 5 months of age
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
shalini ojha
Organizational Affiliation
University of Nottingham
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospitals of Derby and Burton
City
Derby
State/Province
Derbyshire
ZIP/Postal Code
DE3 0ED
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
No

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A Study of Agreement Between Oxygen Saturation Measured by Two Probes in Infants on the Neonatal Unit

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