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NCT05423821 Clinical Trial

Non-operating Room Anesthesia Experiences in Pediatric Magnetic Resonance Imaging Cases

Sedation Complication Clinical Trial

Official title:
Out Patient Anesthesia Experiences in Pediatric Magnetic Resonance Imaging Cases

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT05423821
Other study ID # ytuncdemir-MR
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date June 14, 2022
Est. completion date July 25, 2022

Study information
Verified date June 2022
Source Ankara Training and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

In recent years, out patient anesthesia applications have been increasing for diagnostic and interventional procedures for pediatric patients. In this study, we aimed to retrospectively analyze the anesthesia applications performed in pediatric MRI cases in our hospital. It is a retrospective study

Description:

In recent years, applications with sedation and/or general anesthesia for diagnostic purposes in pediatric cases with Magnetic Resonance Imaging (MRI) method have been increasing. Although imaging methods are useful in diagnosis and treatment, they carry minimal risk for patients. As the demands for anesthesia increase during Magnetic Resonance Imaging, questions have arisen about what can be done safely in anesthesia management. The type of anesthesia applied for Magnetic Resonance Imaging is called non-operating room anesthesia. Cross-sectional imaging techniques such as MRI require pediatric patients to remain calm for up to one hour, and thus these patients need anesthesia. In the induction of anesthesia with agents used in anesthesia outside the operating room, the patient sleeps quickly, the vital functions are stable in its maintenance, the patient recovers quickly after anesthesia, the physical and mental activities return to normal as soon as possible after recovery, and there are no side effects such as nausea, vomiting, dizziness and pain that will delay the discharge. is necessary. Sedation or general anesthesia carries risks and can have unintended consequences if poorly managed.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 350
Est. completion date July 25, 2022
Est. primary completion date July 15, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A to 18 Years
Eligibility Inclusion Criteria: - Elective cases under the age of 18 will be included in the study between 01.01.2020 and 01.01.2022. - Patients to undergo elective magnetic resonance imaging Exclusion Criteria: - Magnetic resonance without anesthesia will not be included. Over the age of 18 will be excluded from study

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Anesthesia efficacy in patients undergoing MRI
atropine will be administered when bradycardia develops, oxygen will be given if hypoxia develops

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Yunus Emre

Outcome
Type Measure Description Time frame Safety issue
Primary The type of anesthesia we trust most in magnetic resonance genel anesthesia two hour
Secondary reducing complications in magnetic resonance mechanical ventilator, endtidal carbon dioxide, non-invasive oxygen saturation two hour
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