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NCT04622436 Clinical Trial

Early Recognition of Hypoxia in Pediatric Patient Sedation

Desaturation of Blood Clinical Trial

Official title:
Comparison of MicroStream Capnography and Pulseoxymeter in Sedation of Pediatric Patients Undergoing Magnetic Resonance Imaging

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT04622436
Other study ID # 2011-KAEK-25 2020/09-03
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date October 1, 2020
Est. completion date April 1, 2021

Study information
Verified date November 2020
Source Bursa Yüksek Ihtisas Education and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Early recognition of hypoxia through monitoring in sedation practices in pediatric patients

Description:

In pediatric Magnetic Resonance Imaging, sedation is applied to pediatric patients of all age groups from newborn to adolescence in order to prevent the anxiety and movement of the patients during the imaging. It was aimed to compare the capnograph and pulse oximeter used for early detection of hypoxia in patient follow-up and to monitor the depth of sedation with the sedation score in the recovery room.

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 4
Est. completion date April 1, 2021
Est. primary completion date April 1, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A to 18 Years
Eligibility Inclusion Criteria: - Patients under 18 years of age who underwent magnetic resonance imaging with sedoanalgesia Exclusion Criteria: - Patients over the age of 18, - Those who do not speak Turkish, - Presence of deformities in the nose and forehead, - Those with nail polish and henna on their nails

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Turkey Bursa Yuksek Ihtisas Education and Research Hospital Bursa Yildirim

Sponsors (1)
Lead Sponsor Collaborator
Bursa Yüksek Ihtisas Education and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary Early recognition of hypoxia The rapid recognition of hypoxia that may occur with the initiation of the procedure during the procedure
Primary the changes in partial oxygen saturation The rapid recognition of changes in partial oxygen saturation during the procedure
Secondary Sedation score Monitoring ramsey sedation scale. The minimum value is 1 and the maximum value is 6. Higher score means more sedatized. during the procedure
Secondary recovery time length of stay in the recovery room immediately after the procedure
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