Skip to main content
Clinical Trials/NCT02676661
NCT02676661
Unknown
Not Applicable

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

Air Force Military Medical University, China1 site in 1 country350 target enrollmentOctober 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Jaw, Edentulous, Partially
Sponsor
Air Force Military Medical University, China
Enrollment
350
Locations
1
Primary Endpoint
peri-implant disease
Last Updated
10 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
October 2014
End Date
December 2022
Last Updated
10 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Air Force Military Medical University, China
Responsible Party
Principal Investigator
Principal Investigator

Ji-hua Chen

Professor and Dean of the Department of Prosthodontics, School of Stomatology, Fourth Military Medical University

Air Force Military Medical University, China

Eligibility Criteria

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.

Outcomes

Primary Outcomes

peri-implant disease

Time Frame: at 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 Outcomes

  • Gingival Bleeding on Probing(at the first day,6 months 1,3 and 5 years after prosthetic loading.)
  • Pocket depths(at the first day,6 months 1,3 and 5 years after prosthetic loading.)
  • Marginal bone loss(at the first day,6 months 1,3 and 5 years after prosthetic loading.)

Study Sites (1)

Loading locations...

Similar Trials