Effects of Platelet-rich-fibrin on Post-surgical Complications of Impacted wisdom tooth surgery
Phase 3
Recruiting
- Conditions
- Platelet-rich fibrin.
- Registration Number
- IRCT20201227049849N1
- Lead Sponsor
- Kashan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
Adults
Patients with bilateral inter-bone impacted wisdom tooth
Exclusion Criteria
Pregnancy
Lactation
Having pre-operative sign or symptom
Existence of pathology in impaction area
Allergy to Penicillin, Paracetamol, chlorhexidine
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Post-operative pain degree. Timepoint: First 7 days after surgery. Method of measurement: 0-10 Numeric Pain Rating Scale.;Post-operative edema amount. Timepoint: 1,3 and 7 days after surgery. Method of measurement: The distance between tragus and mouth commissure in horizontal plane and the distance between lateral cantus and gonion in vertical plane, would be measured by a flexible band.;Post-operative bleeding amount. Timepoint: 3 and 7 days after surgery. Method of measurement: Massive, uncontrollable bleeding since 2nd day of surgery would be conformed by patient.;Post-operative infection manifestation. Timepoint: 4- 7 days after surgery. Method of measurement: Assessment of pus discharge, redness and temperature increasing after the 3rd day after surgery.;Post-operative dry socket manifestation. Timepoint: 4- 7 days after surgery. Method of measurement: Presence of extreme pain not being decreased by taking analgesics and empty socket without pus discharge or fever.
- Secondary Outcome Measures
Name Time Method