Increase in short dental implant primary stability with Osseodensification: a split-mouth clinical study
- Conditions
- Tooth Loss
- Registration Number
- RBR-8mk389h
- Lead Sponsor
- Faculdade de Odontologia de Bauru da Universidade de São Paulo
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruitment completed
- Sex
- Not specified
- Target Recruitment
- Not specified
Healthy participants of both sexes; at least 18 years old; that present at least 2 edentulous sites with a minimum bone height of 10 mm and a minimum cervical bone thickness of 5 mm; minimum age of 18 years; ASA I or ASA II patients - American Society of Anesthesiologists; healthy adjacent teeth or without the need for prosthetic restoration; patients who have signed the Free and Informed Consent Form (TCLE)
History of alcoholism; smokers; illicit drug users; heart disease; decompensated diabetics; complex rehabilitation needs (change in the vertical dimension of occlusion, need for other rehabilitation procedures); lack of sufficient height and bone thickness; carriers of parafunctional habits (bruxism); grafted areas; irradiated patients; patients who have undergone long-term steroid treatment or bisphosphonate users
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method It is expected an improvement in the primary stability of dental implants when submitted to the osseodensification technique
- Secondary Outcome Measures
Name Time Method There are no secondary outcomes expected