effects of propofol/apotel and propofol/fentanyl on dental sedation of 2-6 years old uncooperative childre

Phase 3

• Conditions: F06.4; Anxiety.; Anxiety disorder due to known physiological condition

• Registration Number: IRCT20221203056700N1
• Lead Sponsor: Shahid Beheshti University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 7 February 2023

Recruitment & Eligibility

• Status: Pending
• Sex: All
• Target Recruitment: 38

Inclusion Criteria

2-6 years old children
Uncooperative
Need to at least two same and symmetric treatment session
ASA 1 health status

Exclusion Criteria

The age under 2 and above 6 years
Cooperative
Lack of similar treatment needs
ASA 2 and more

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Conscious sedation. Timepoint: Venipuncture, local anesthesia and Every 15 minutes. Method of measurement: Houpt scale.

Secondary Outcome Measures

Name	Time	Method
SPO2. Timepoint: Venipuncture, local anesthesia and every 15 minutes. Method of measurement: Pulse oximeter.;Heart rate. Timepoint: Venipuncture, local anesthesia and every 15 minutes. Method of measurement: Pulse oximeter.