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Evaluation of the Effects Using the Combination of Sedative Agents on Dental Anxiety in Pediatric Patients

Anxiety Postoperative Clinical Trial

Official title:
Çocuk Hastalarda Değişik Konsantrasyonlarda Kullanılan Sedasyon Ajanlarının Anksiyete Üzerine Etkilerinin Değerlendirilmesi

Clinical Trial Summary

The aims of this study were firstly, to evaluate the changes in the anxiety level after deep sedation with various intravenous sedative agents using salivary cortisol level in pediatric dental patients and secondly, to compare clinical effectiveness of this sedative agents, perioperative complications, recovery time and adverse effects.

Clinical Trial Description

This clinical study was included 69 healthy pediatric patients aged 3 to 7 years with high anxiety. The patients were divided into 3 groups according to the sedative agents: Group 1 (n=23) was received Propofol, Group 2 (n=23) was receieved Ketofol 1:3, and Group 3 (n=23) was received Ketofol 1:4. The anxiety levels were assessed using Facial Image Scale (FIS) anxiety scale and changes in salivary cortisol levels were assessed using ELISA before and after the drug administration. Perioperative vital signs, depth of sedation were recorded at intervals of 5 minutes. Preoperative and postoperative complications, operation and recovery time were recorded in the follow-up form. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04623970
Study type Interventional
Source Cukurova University
Contact
Status Completed
Phase N/A
Start date November 28, 2018
Completion date October 5, 2020
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