Non-operating Room Anesthesia Experiences in Pediatric Magnetic Resonance Imaging Cases
NCT ID: NCT05423821
Last Updated: 2022-06-21
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
350 participants
OBSERVATIONAL
2022-06-14
2022-07-25
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
It is a retrospective study
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
The Incidence and Nature of Adverse Events During Pediatric Sedation for MRI/CT in One Korean University Hospital: Retrospective Study
NCT01855581
The Incidence and Nature of Adverse Events During Pediatric Sedation for MRI/CT in One Korean University Hospital: Prospective Study
NCT01855555
Oral Dexmedetomidine in Pediatric MRI
NCT05619627
Safety Evaluation of Propofol Sedation for Magnetic Resonance Imaging in Pediatric Patients
NCT04455776
Sedation MRI - Propofol Versus Propofol-Ketamin in Children
NCT01519154
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
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.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_ONLY
RETROSPECTIVE
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Anesthesia efficacy in patients undergoing MRI
atropine will be administered when bradycardia develops, oxygen will be given if hypoxia develops
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Patients to undergo elective magnetic resonance imaging
Exclusion Criteria
1 Day
18 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Yunus Emre
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Yunus Emre
SPECIALIST DOCTOR
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
ytuncdemir-MR
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.