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Comparative study of Cerebral oxygen saturation using multi-oxygenation probe and other cerebral oximeter

Not Applicable
Conditions
Not Applicable
Registration Number
KCT0005859
Lead Sponsor
Korea University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot yet recruiting
Sex
All
Target Recruitment
16
Inclusion Criteria

1. Healthy adult (20-45 years old)
2. No comorbidities
3. Agreement with informed consent for participating to the study

Exclusion Criteria

1. Hypertension, diabetes, cerebrovascular disease, cardiac disease, chronic respiratory disease, hemodynamic disease including anemia
2. Patients with skin-color difference that might affect light absorption, such as jaundice
3. Smokers
4. Patients with possible difference between both cerebral hemispheres due to history of head trauma, stroke, carotid artery surgery or cardiac surgery.
5. Pregnant women, patients with skin reaction, foreigners etc.

Study & Design

Study Type
Interventional Study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
?Evaluating the agreement of levels of cerebral oxygen saturation between comparator group (O3 Regional oximeter module, Masimo, USA) and experimental group (VP1200+Votem sensor, Votem, Korea) Using Bland–Altman plot (95% limit of agreements ± 1.96 standard deviation)
Secondary Outcome Measures
NameTimeMethod
?Analysis of time-serial differences of levels of cerebral oxygen saturation among comparator group (O3 Regional oximeter module, Masimo, USA) and experimental group (VP1200+Votem sensor, Votem, Korea) Using Repeated measured ANOVA
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