Frequency of Adverse Events in Pediatric Patients Receiving Sedation for Magnetic Resonance Imaging

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age0-16
SponsorSisli Hamidiye Etfal Training and Research Hospital

About this trial

Introduction:The application of anesthesia outside the operating room for pediatric patients has increased in recent years. For diagnostic and treatment follow-up purposes, magnetic resonance imaging (MRI) requires the pediatric patient to remain still, necessitating sedation. The study aimed to determine the frequency of adverse effects and influencing factors in pediatric patients undergoing sedation during MRI.

Methods: Between 19.06.2024 and 16.09.2024, estimated 500 pediatric patients who underwent MRI under sedation will be prospectively observed. All non-intubated patients under the age of 16 will be included in the study. The demographic data, comorbidities, and medications of the patients, the procedures performed, the anesthetic drugs used, the expertise duration of the anesthesiologist, and the adverse effects encountered will be recorded.

Eligibility criteria

Qualifiers

All non-intubated patients under the age of 16 were included in the study.

Disqualifiers

Intubated pediatric patients or older than 16 years patients were excluded.

Trial design

Treatments tested in this trial

  • Pediatric patients who received sedation for magnetic resonance imaging

Treatment groups

500 Participants
are divided into 1 treatment group