The effect of premedication with an antidepressant before surgery of impacted mandibular third molar on pain control
Phase 3
- Conditions
- Impaction of mandibular third molar.
- Registration Number
- IRCT20240419061526N1
- Lead Sponsor
- Tabriz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
Participants with similar impacted third mandibular molars on both left and right sides with similar impaction pattern
Participants with informed consent to participate in the study
Participants with no inflammatory symptoms in the oral cavity such as tooth decay and advanced periodontal diseases
Exclusion Criteria
Participants who are unwilling to participate in the study
Pregnancy
Taking pain-relieving drugs two weeks before surgery
Allergy to amitriptyline
Systemic disorders that are contraindications for surgery, such as high blood pressure and uncontrolled diabetes
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain intensity of patients after surgery. Timepoint: Measuring the pain level of patients every 6 hours after surgery up to 24 hours. Method of measurement: Visual Analogue Scale.
- Secondary Outcome Measures
Name Time Method