Evaluation of Local and Systemic Laser Application in Dental Implant Surgery: Clinical study
- Conditions
- AnodontiaC05.500.480.450
- Registration Number
- RBR-7f42fs5
- Lead Sponsor
- Pontifícia Universidade Católica de Campinas
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- Not specified
Patients over 18 years of age with an indication for dental implants will be included in the study according to the following inclusion criteria: Patients with an indication for upper (maxilla) and/or lower (mandible) single dental implants in healed sockets (at least 60 days after extraction); Healthy oral mucosa. A prior clinical analysis will be carried out and the patient must present no mucosal disease, that is, no phlogistic (inflammatory) and infectious signs; Patients who agree to participate in the research by signing the Informed Consent Form
Patients with systemic diseases, such as: diabetes mellitus, cardiovascular diseases, coagulation disorders, osteoporosis and/or hypertension; Patient undergoing radiation to the head or neck; Patients with a history of implant loss; Pregnant or lactating women; Sensitivity to light (photophobia); Smokers and alcohol addicts; Patients using medications that alter bone metabolism, such as: heparin, warfarin, cyclosporine, glucocorticoids, medroxyprogesterone acetate, oncological medications, thyroid hormone, prednisone, prednisolone, methylprednisolone, dexamethasone, cortisone and triamcinolone; Patients who have been or are being treated with antibiotics or anti-inflammatories for less than 2 weeks
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method