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Clinical Trial Summary

Investigation of the effect of preoperative anxiety on postoperative delirium in children who will undergo circumcision operation


Clinical Trial Description

In order to determine the effect of circumcision on preoperative anxiety and postoperative delirium, patients will be divided into two groups who will undergo circumcision surgery and who will undergo inguinal hernia surgery.

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 ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04009200
Study type Observational [Patient Registry]
Source Ankara Diskapi Training and Research Hospital
Contact
Status Completed
Phase
Start date March 1, 2018
Completion date December 15, 2019

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