Sedative effect of ketamine / propofol and ketamine / midazolam on non-cooperating children in pediatric dentistry

Phase 3

Recruiting

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

• Registration Number: IRCT20090506001882N10
• 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: 26 April 2021

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

Be in the negative group be Frankel's behavioral classification.
Requires at least 2 similar treatment sessions.
Be in the ASAI group.
Be 2 to 6 years old.

Exclusion Criteria

Suffering Systemic Disease..
Colds during in treatment session.
Non-prescription medication including allergies and treatment needs different from protocol.

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Conscious sedation. Timepoint: Every 15 minutes. Method of measurement: Houpt scale.

Secondary Outcome Measures

Name	Time	Method
SpO2. Timepoint: Every 15 minutes. Method of measurement: Pulse oximeter.;Heart rate. Timepoint: Every 15 minutes. Method of measurement: Pulse oximeter.