Effect of Dexmedetomidine on patient's sedation and surgeon's satisfaction during wisdom tooth surgery
- Conditions
- Mandibular impacted wisdom tooth.Impacted teethK01.1
- Registration Number
- IRCT20200406046966N1
- Lead Sponsor
- Esfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 26
According to the ASA physical status classification system, patient should be ASA I or ASA II (normal healthy patient or patient with mild systemic disease).
Patient with informed consent.
Patient's age should be between 18-30 years.
Patients should have two wisdom teeth (classified in the same class by Pell & Gregory; mesioangular impaction, level B, class 1 or 2), which are similar in terms of surgical severity;
No general contraindications (in these patients use of dexmedetomidine is contraindicated: patients with low blood pressure, bradycardia, sinus disorder, unstable high blood pressure, arousability, tachyphylaxis and liver disorders.)
No lesions and malignancies at the surgical site;
No smoking.
Patient with wisdom tooth surgery on one side;
Occurring medical problems during surgery;
Patient who needs more than one cartridge injection;
Surgery lasting more than 20 minutes.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The patient's sedation rate. Timepoint: After the intervention. Method of measurement: Short Dental Fear Questionnaire.;Surgeon's satisfaction. Timepoint: After the intervention. Method of measurement: Visual Analogue Scale.
- Secondary Outcome Measures
Name Time Method Patient's cooperation level. Timepoint: After the intervention. Method of measurement: Data collection form.;Evaluation of patient's satisfaction. Timepoint: After the intervention. Method of measurement: Visual Analogue Scale.