Osseointegration
Conditions
Interventions
this split-mouth randomized clinical trial analyzed the insertion of 30 implants in the posterior region of the mandible of 15 patients, comparing the implant stability quotient values of two groups o
Sponsors
pontifícia universidade católica do paraná
pontifícia universidade católica do paraná
Eligibility
Age
21 Years to No maximum
Inclusion criteria
Inclusion criteria: partial edentulous patients in the posterior region of the mandible requiring one implant in each half-arch or two implants in each half-arch;minimum bone height of 11 mm and minimum bone thickness of 5 mm in the posterior region of the bilateral mandible evaluated by means of cone beam computed tomography; sufficient prosthetic space for subsequent prosthetic rehabilitation
Exclusion criteria
Exclusion criteria: the need for some type of bone reconstruction or advanced surgery to allow the installation of the implant; patients who did not accept to be part of the study; patients with uncontrolled diabetes, considering glycated hemoglobin above 7.5%; smokers more than 10 cigarettes a day; use of oral or injectable bisphosphonates; immunodeficient patients; patients who underwent radiotherapy in the head and neck region for a period of less than five years before the beginning of the research; patients with another systemic condition that contraindicated performing oral surgery at the time or who had conditions that could interfere with the osseointegration process
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Expected outcome 1: the ISQ (implant stability quotient) value at the end of 42 days was expected to be higher in the test group than in the control group.;Outcome found 1: The ISQ (implant stability quotient) value at the end of 42 days had no significant difference between the tested groups. | — |
Countries
Brazil
Contacts
Public ContactPatricia Souza
Pontifícia Universidade Católica do Paraná
Outcome results
None listed