Pediatric Brain Tumor, Pediatric Cancer, Pediatric Solid Tumor
Conditions
Keywords
Magnetic Resonance, sedation, maternal voice, sedative effects
Brief summary
To evaluate the effects of music and maternal voice in children on sedation depth and sedative use during pediatric magnetic resonance imaging.
Detailed description
When the patients and their parents arrived in the magnetic resonance unıt about 30 minutes before the procedure, the anesthetist is obtained a medical history and carried out a physical examination and clinical assesment. Patients were categorized into 3 groups: music, maternal voice and isolation. During the procedures,the patients in the music group listened to Vivaldi's The Four Seasons violin concertos by sound isolating headphones, whereas the patients in the isolation group wore the headphones but did not listen to music. All patients were sedated by midazolam and propofol. During the procedure, an additional propofol was administered as required
Interventions
PROCEDUREGroup headphone
The patients in the first group wore the headphones but did not listen the music or maternal voice. The standard sedation method was applied to all patients.
PROCEDUREGroup music
The patients in the second group listened to classical music (Vivaldi's The Four Seasons violin concertos) by sound- isolating headphones through the procedure.The standard sedation method was applied to all patients.
PROCEDUREGroup maternal voice
The patients in the third group listened to maternal voice by sound- isolating headphones through the procedure.The standard sedation method was applied to all patients.
Sponsors
TC Erciyes University
Study design
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
DIAGNOSTIC
Masking
SINGLE (Subject)
Eligibility
Sex/Gender
ALL
Age
3 Years to 12 Years
Healthy volunteers
Yes
Inclusion criteria
* ASA (American Society of Anesthesiologists) I-II
Exclusion criteria
* Patients with hearing impairment, distorted ear anatomy, recent organ or system deficiency, severe pulmonary and/or cardiovascular problems, intolerance to propofol, airway ab-normalities, or known psychiatric or mental problems were ex-cluded from the study.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| amount of propofol dose used in sedation | during the MRI procedure | The total propofol dosage were recorded in during procedure. |
Countries
Turkey (Türkiye)
Outcome results
None listed