periimplantitis
Conditions
Interventions
This is a two-arm, double-blind, randomized controlled clinical study. A total of 30 people who meet the eligibility criteria will be randomly allocated to one or another intervention group using a co
Sponsors
Universidade Estadual Paulista, Faculdade de Odontologia de Araraquara, FOAR-UNESP
Universidade Estadual Paulista, Faculdade de Odontologia de Araraquara, FOAR-UNESP
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Greater than or equal to eighteen years of age; greater than or equal to three radiographic bone loss ; greater than or equal to six millimeters of probing pocket depth with bleeding on probing; less than or equal to twenty percent of plaque index; less than or equal to twenty percent of gingival index ; formal consent to participate in the research
Exclusion criteria
Exclusion criteria: Presence of uncontrolled systemic alteration; use of medications six months prior to the study that may influence the response to treatment; pregnant and lactating women, performing peri-implant treatment including subgingival instrumentation in the six weeks prior to the study; implants with mobility; oral pathology; history of allergy to any component of the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to find a gain in radiographic bone filling of at least 1mm through linear measurements using the implant platform and the bottom of the defect as reference points using the ImageJ program. | — |
Secondary
| Measure | Time frame |
|---|---|
| It is expected to find a reduction on probing pocket depth of at least 1mm through clinical measurements using a periodontal probe from gingival margin to the bottom of the implant pocket as reference points. | — |
Countries
Brazil
Contacts
Public ContactJavier Vivanco
Universidade Estadual Paulista, Faculdade de Odontologia de Araraquara, FOAR-UNESP
Outcome results
None listed