Tomographic evaluation of Prosthesis-Guided after Tooth Extractio
Not Applicable
- Conditions
- Bone RegenerationK08.1
- Registration Number
- RBR-7tkkqj4
- Lead Sponsor
- niversidade Do Grande Rio-Unigranrio
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruitment completed
- Sex
- Not specified
- Target Recruitment
- Not specified
Inclusion Criteria
Healthy volunteers; both genders; non smokers; age between 18 and 60 years; indication of extraction of at least one tooth; gingival margin in harmony with the gingival margins of neighboring teeth; proximal bone crests of neighboring teeth compatible with normal periodontium.Total sample of 20 teeth
Exclusion Criteria
Smoking volunteers; diagnoses of hematological or metabolic pathologies; use of bisphosphonates or any medication that interferes with bone healing; diseases that compromise the immune system; patients undergoing radiotherapy in the head and neck region; pregnant or lactating women; untreated periodontal disease
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The bone thickness will be evaluated in mm, using tomographies, initial and after the treatment. With the help of a software that will calculate this measurement on video. For this parameter, bone thickness is expected as the primary outcome at the end of the study.
- Secondary Outcome Measures
Name Time Method The secondary outcome evaluated will be the analysis of the percentage of tissues (mature or immature bone) and fibrous connective tissue will be performed in micrometers, evaluating the histological section of the central section of the bone removed for implant installation. No other secondary outcome related to another event ,variable or different experience is expected in any different time period.