Evaluation of Pregabalin oral sedation in impacted third molar surgery .
Phase 2
- Conditions
- Impacted third molar surgery.
- Registration Number
- IRCT201212241674N6
- Lead Sponsor
- Vice-Chancellery of Research and Technology, Shiraz University Of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 210
Inclusion Criteria
Inclusion criteria included : Older than 18 and younger than 51 years old ? ASA physical status I (without diseases) were selected ? and Exclusion criteria included: underlying disease ? Obesity (weight more than 20% above ideal weight ? Short stature (less than 140 cm) ? A history of anti-epileptic drugs or alcohol addiction ? History of allergy to opioids ? Renal dysfunction ? Nervous system diseases ? Cardiovascular diseases ? History of chronic pain and anticonvulsant drugs .
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Measurement of blood pressure and heart rate. Timepoint: One hour before surgery , end of surgery and during discharge. Method of measurement: Digital blood pressure measuring device.;Measure the level of sedation. Timepoint: before surgery , end of surgery and during discharge. Method of measurement: Ramsay Sedation Scale.
- Secondary Outcome Measures
Name Time Method Patient's satisfaction. Timepoint: end of surgery. Method of measurement: ranking from excellent, very good, good, average, poor.;Dentist' satisfaction from cooperation of the patient. Timepoint: end of surgery. Method of measurement: ranking from excellent, very good, good, average, poor.