- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06626763
Comparison of Oxygen Saturation Measurements Using Different Glove Colors in Children
October 3, 2024 updated by: ELİZ GECTAN, Izmir Katip Celebi University
Comparison of Oxygen Saturation Measurements Using Different Glove Colors in Children: A Preventive Method for Infection?
The aim of this study was to determine the effect of different colored gloves on oxygen saturation in pediatric patients whose oxygen saturation was measured by pulse oximetry in pediatric emergency department.
The population of the study, which is planned as a prospective cohort study, will consist of children between the ages of 3-18 years who underwent oxygen saturation measurements in the pediatric emergency clinic of İzmir Bakırçay University Cigli and Training and Research Hospital between October 2024 and October 2025.
Study Overview
Status
Not yet recruiting
Conditions
Detailed Description
The aim of this study was to determine the effect of different colored gloves on oxygen saturation in pediatric patients who underwent oxygen saturation measurement by pulse oximetry in pediatric emergency department.
The population of the study, which is planned as a prospective cohort study, will consist of children aged 3-18 years who underwent oxygen saturation measurements in the pediatric emergency clinic of İzmir Bakırçay University Çiğli and Training and Research Hospital between October 2024 and October 2025.
The sample of the study will consist of children who meet the inclusion criteria on the specified dates and whose parents/legal guardians agree to participate in the study.
Descriptive Characteristics Form and Oxygen Saturation Measurement Value Record Form will be used for data collection.
Study Type
Observational
Enrollment (Estimated)
68
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Eliz Geçtan
- Phone Number: 05451342435
- Email: elizgectan09@gmail.com
Study Locations
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Izmir, Turkey
- İzmirKCU
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
Children between the ages of 3-18
Description
Inclusion Criteria:
- Children between the ages of 3-18,
- The parent/legal guardian or the child himself/herself agrees to participate in the study,
- Arterial blood gas measurement was performed,
Exclusion Criteria:
- The finger has a skin condition,
- Having nail polish on your fingernails,
- Having a severed finger,
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Experimental
Children will be measured 5 times using a pulse oximeter.
The measurements will be performed consecutively without any interval between them.
The first measurement will be performed without using any gloves on the patient's finger, the second measurement will be performed using transparent gloves, the third measurement will be performed using white gloves, the fourth measurement will be performed using black gloves, and the fifth measurement will be performed using blue gloves.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Measuring the arterial blood gas SpO2 saturation
Time Frame: Procedure
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Finger SpO2 measurements will be initiated as soon as the blood gas measurement process starts.
Pulse oximetry measurements and intra-arterial blood gas measurements will be performed
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Procedure
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without gloves measuring the SpO2 saturation
Time Frame: While the patient was not wearing gloves, the pulse oximeter light source was placed on the outer surface of the finger. SpO2 was read after waiting an average of 30 seconds.
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While the patient was not wearing gloves, the pulse oximeter light source was placed on the outer surface of the finger. SpO2 was read after waiting an average of 30 seconds.
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SpO2 saturation measurement with transparent colored glove
Time Frame: While the patient was wearing a transparent glove, the pulse oximeter light source was placed on the outer surface of the finger. SpO2 was read after waiting an average of 30 seconds.
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While the patient was wearing a transparent glove, the pulse oximeter light source was placed on the outer surface of the finger. SpO2 was read after waiting an average of 30 seconds.
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SpO2 saturation measurement with white colored glove
Time Frame: While the patient was wearing a white glove, the pulse oximeter light source was placed on the outer surface of the finger. SpO2 was read after waiting an average of 30 seconds.
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While the patient was wearing a white glove, the pulse oximeter light source was placed on the outer surface of the finger. SpO2 was read after waiting an average of 30 seconds.
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SpO2 saturation measurement with black colored glove
Time Frame: While the patient was wearing a black glove, the pulse oximeter light source was placed on the outer surface of the finger. SpO2 was read after waiting an average of 30 seconds.
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While the patient was wearing a black glove, the pulse oximeter light source was placed on the outer surface of the finger. SpO2 was read after waiting an average of 30 seconds.
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SpO2 saturation measurement with blue colored glove
Time Frame: While the patient was wearing a blue glove, the pulse oximeter light source was placed on the outer surface of the finger. SpO2 was read after waiting an average of 30 seconds.
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While the patient was wearing a blue glove, the pulse oximeter light source was placed on the outer surface of the finger. SpO2 was read after waiting an average of 30 seconds.
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
October 8, 2024
Primary Completion (Estimated)
October 8, 2025
Study Completion (Estimated)
October 8, 2025
Study Registration Dates
First Submitted
September 29, 2024
First Submitted That Met QC Criteria
October 3, 2024
First Posted (Actual)
October 4, 2024
Study Record Updates
Last Update Posted (Actual)
October 4, 2024
Last Update Submitted That Met QC Criteria
October 3, 2024
Last Verified
October 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 1753
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.