The Effect of Preoperative Anxiety on Postoperative Delirium in Children
NCT ID: NCT04009200
Last Updated: 2020-01-14
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
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COMPLETED
60 participants
OBSERVATIONAL
2018-03-01
2019-12-15
Brief Summary
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Detailed Description
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Modified Yale Preoperative Anxiety Scores (m-YPAS), Visual Analogue Scale Anxiety (VAS-anxiety) will be evaluated when patients are taken to the preoperative waiting room.
After awakening, patients will be taken to the postoperative wake-up room where Pediatric Anesthesia Recovery Delirium Scores (PAED), Recovery Agitation 5-point Scores (EA), FLACC scores will be evaluated every 5 minutes and mean arterial pressure, pulse, SPO2 values will be recorded. Duration of stay in recovery unit will be recorded
Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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circumcision
Modified Yale Preoperative Anxiety Scores (m-YPAS), Visual Analogue Scale Anxiety (VAS-anxiety) will be evaluated when patients are taken to the preoperative waiting room.
After awakening, patients will be taken to the postoperative wake-up room where Pediatric Anesthesia Recovery Delirium Scores (PAED), Recovery Agitation 5-point Scores (EA), FLACC scores will be evaluated every 5 minutes and mean arterial pressure, pulse, SPO2 values will be recorded. Duration of stay in recovery unit will be recorded
No interventions assigned to this group
inguinal hernia
Modified Yale Preoperative Anxiety Scores (m-YPAS), Visual Analogue Scale Anxiety (VAS-anxiety) will be evaluated when patients are taken to the preoperative waiting room.
After awakening, patients will be taken to the postoperative wake-up room where Pediatric Anesthesia Recovery Delirium Scores (PAED), Recovery Agitation 5-point Scores (EA), FLACC scores will be evaluated every 5 minutes and mean arterial pressure, pulse, SPO2 values will be recorded. Duration of stay in recovery unit will be recorded
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Elective circumcision or elective inguinal hernia
Exclusion Criteria
* Development disability
* Prematurity
* Neurological diseases
* Psychoactive medication use
* Hearing/ visual impairment
* History of surgery
6 Years
10 Years
MALE
No
Sponsors
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Ankara Diskapi Training and Research Hospital
OTHER
Responsible Party
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ilkay baran akkuş
specialist doctor
Principal Investigators
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Ilkay Baran Akkuş
Role: PRINCIPAL_INVESTIGATOR
Diskapi Yildirim Beyazit Training Education Hospital
Locations
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Diskapi Yildirim Beyazit Training Research Hospital
Ankara, Altındag, Turkey (Türkiye)
Countries
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Other Identifiers
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44/07
Identifier Type: -
Identifier Source: org_study_id
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