Investigating the effect of amoxicillin in reducing infection after impacted wisdom tooth surgery
Phase 3
Recruiting
- Conditions
- .
- Registration Number
- IRCT20200705048014N2
- Lead Sponsor
- Bandare-abbas University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
All patients between the ages of 18 and 60, of both sexes, without systemic problems, who refer for mandibular wisdom tooth surgery.
Exclusion Criteria
The patient's lack of consent to cooperate
receiving antibiotics in the last three months
Failure to strictly follow the instructions after the operation
Patients who have unusual problems during tooth extraction
Existence of systemic diseases and pregnant women
Presence of infection in the patient
The patient's sensitivity to amoxicillin
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Wound healing process. Timepoint: 7 days after surgery. Method of measurement: Clinical examination of the wound.;Pain after surgery. Timepoint: Daily up to 7 days after surgery. Method of measurement: Question from the patient and rating from 1 to 5.
- Secondary Outcome Measures
Name Time Method Erythema in the area. Timepoint: 7 days after surgery. Method of measurement: Physical examination.;Halitosis. Timepoint: Daily until seven days after surgery. Method of measurement: Ask the patient.;Trismus. Timepoint: 7 days after surgery. Method of measurement: Clinical examination using a ruler with millimeter unitsCommunity Verified icon.