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Evaluation of the Prevalence and Risk Factors for Patients With Peri-implant Disease

The Prevalence and Risk Factors for Patients With Peri-implant Disease: A Prospective Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02676661
Enrollment
350
Registered
2016-02-08
Start date
2014-10-31
Completion date
2022-12-31
Last updated
2016-02-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Jaw, Edentulous, Partially

Keywords

peri-implant disease, risk factors, prevalence

Brief summary

To investigate the prevalence and risk factors for peri-implant disease in partially edentulous patients rehabilitated with implants supported crown or bridge so as to provide evidence for clinical prevention and control.

Detailed description

The aim of the present study is to identify the prevalence of peri-implant disease in partially edentulous subjects treated with osseointegrated implants, using clinical parameters, as well as to analyse the possible disease association with demographic, behavioural, and biological risk variables.

Interventions

None listed

Sponsors

Air Force Military Medical University, China
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
Yes

Inclusion criteria

* Partially edentulous patients will implant at least one implant and will be restored with implant-supported fixed partial dentures and single crowns.

Exclusion criteria

* Jaw radiotherapy treatment before and after implanting. Patients who have bruxism,xerostomia or the adjacent teeth periapical periodontitis. * Patients who suffered with oral mucosa disease,or aggressive periodontitis or jaw defect. * Patients who suffered with mental and psychological disease will influence their oral health normal maintenance.

Design outcomes

Primary

MeasureTime frameDescription
peri-implant diseaseat the 5 years after prosthetic loading.Peri-implant disease includes Peri-implant mucositis and Peri-implantitis.Peri-implant mucositis: BoP/suppuration but no detectable bone loss. Peri-implantitis: BoP/suppuration and bone loss \>2 mm.

Secondary

MeasureTime frameDescription
Gingival Bleeding on Probingat the first day,6 months 1,3 and 5 years after prosthetic loading.Gingival bleeding on probing (BOP) using the modified sulcus bleeding index for implants. Scale equals 0 = No bleeding when periodontal probe is passed along the gingival margin;1 = Isolated bleeding spots visible;2 = Blood forms a confluent red line on the gingival margin;3 = Heavy or profuse bleeding.
Pocket depthsat the first day,6 months 1,3 and 5 years after prosthetic loading.PD will be measured from the free gingival margin to the base of the pocket and will be recorded in whole millimeters (mm).
Marginal bone lossat the first day,6 months 1,3 and 5 years after prosthetic loading.Marginal bone loss will be assessed by periapical radiographs taken with the paralleling technique.

Countries

China

Contacts

Primary ContactJihua Chen, PhD
jhchen@fmmu.edu.cn029-84776329
Backup ContactMin Tian, PhD
tianminno1@163.com029-84776129

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026