se of the Laser to improve the post-operative of the Tooth Removal Surgery
- Conditions
- Included teethCID 10 - K01.0
- Registration Number
- RBR-10kqbm9f
- Lead Sponsor
- niversidade Estadual Paulista Julio de Mesquita Filho (Unesp) - Faculdade de Odontologia de Araçatuba (FOA)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruitment completed
- Sex
- All
- Target Recruitment
- Not specified
Healthy patients; aged between 18 and 35 years; both genders; good systemic and local health condition; with precise indication for extraction of bilateral lower third molars (38 and 48); third molars in the mesio-angular, vertical or horizontally included or semi-included positions; third molars with fully formed root; same pattern of impaction and position on both sides of the mandible.
Patients using any systemic medication; who had any changes, such as diabetes, systemic arterial hypertension, hyperthyroidism, osteoporosis, gastrointestinal diseases, or any other changes that could compromise the outcome of the surgery or against indicating it; mandibular third molars in position C; local changes such as pericoronitis, odontogenic cysts and tumors associated or not with the third molar, trauma in the region, or presence of infection; patient with allergies to the analgesic aid offered in the postoperative period; allergies to PVPI antisepsis solution 0.12% chlorhexidine gluconate solution; allergy to 2% lidocaine hydrochloride with epinephrine 1: 100,000.
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate the control of PAIN verified by the Number of Painkillers Consumed and by the visual analog scale (VAS);To evaluate the control of EDEMA assessed by visual analog scale (VAS) and by facial measurements;To evaluate the TRISM presence through the mouth opening reduction
- Secondary Outcome Measures
Name Time Method Secondary outcomes are not expected