Two techniques for osseous preservation after tooth extracton: a clinical study
- Conditions
- bone remodelingE04.680.300.500, E06.645.410, E06.721.485
- Registration Number
- RBR-6nrnk9
- Lead Sponsor
- niversidade Federal do Rio Grande do Sul
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- Not specified
- Target Recruitment
- Not specified
Individuals with 18 years-old or older and periodontally healthy; less than 10 percent bleeding on probing without obvious periodontal pockets; present a non-molar tooth with extraction indicated; Type II or I sockets; Present a cone beam computed tomography (up to 1 month) of the region; No history of systemic diseases that contraindicate the surgical procedure, including the need for antibiotic prophylaxis; Do not use continuous use drugs including anti-inflammatory steroids and non-steroids; Present at least two tooth adjacent to the element that will be extracted; Not be pregnant or breastfeeding.
Not able to attend postoperative evaluations; Presenting symptoms of infection or hypersensitivity in the operated area; Smokers or ex-smokers (less than one year); Patients with fractures of the vestibular bone at the time of extraction with more than 50% loss of vestibular wal; Extractions with complications/accidents lasting more than 45 minutes
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To Evaluate Hard Tissue Changes by CBCT, measured by area percentage <br>;To evaluate Soft Tissue Changes by Digital Scanning, measured by area percentage <br>
- Secondary Outcome Measures
Name Time Method Postoperative pain levels assessed by a Visual Analogue Scale (VAS) <br>;VAS scores for swelling and bleeding ;To evaluate Oral Health related quality of life with Oral Health Impact Profile (OHIP14)