Evaluation of propofol / ketorolac / Apotel sedation with intravenous propofol / fentanyl in dental treatment of uncooperating childre
Phase 3
Recruiting
- Conditions
- Anxiety.Anxiety disorder due to known physiological conditionF06.4
- Registration Number
- IRCT20090506001882N11
- Lead Sponsor
- Shahid Beheshti University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
Be in the negative group of 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.