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Prevalence and Risk Indicators of Peri-implant Diseases in China

Prevalence and Risk Indicators of Peri-implant Diseases in China: A Multicenter Cross-sectional Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06208254
Enrollment
500
Registered
2024-01-17
Start date
2024-01-31
Completion date
2025-01-31
Last updated
2024-01-17

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

Conditions

Peri-Implantitis

Brief summary

The goal of this multicenter cross-sectional study is to investigate the prevalence of peri-implantitis in China. The main questions it aims to answer are: * What is the prevalence of peri-implantitis in China * What are the risk indicators of peri-implantitis in China Participants will be invited to a free-of-charge clinical and radiographic examination of conventional dental implants present for over 5 years.

Interventions

None listed

Sponsors

Dalian Medical University
CollaboratorOTHER
Nanchang University
CollaboratorOTHER
Ningxia Medical University
CollaboratorOTHER
Shanxi Medical University
CollaboratorOTHER
Hospital of Stomatology, Wuhan University
CollaboratorOTHER
Hospital of Stomatology, Sun Yat-Sen University
CollaboratorOTHER
Zunyi Medical College
CollaboratorOTHER
Hong Kong Brånemark Osseointegration Center
CollaboratorOTHER
Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University
Lead SponsorOTHER

Study design

Observational model
ECOLOGIC_OR_COMMUNITY
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Patients having at least one rough surface titanium implant in function for more than 5 years 2. Patients treated between January 1, 2013 and December 31, 2017 3. All the implants osseointegrated in the patients' mouth at the time of the examination (including those placed in external clinics) and having at least 5 years of loading, either proven by dental charts or confirmed by the patients, were evaluated

Exclusion criteria

1. Selected patients were invited to participate in the study by telephone calls on the numbers reported in their medical records, and if no response, the patient was not discarded until at least five attempts on different days have been made 2. Periapical and/or panoramic radiographs unavailable 3. History of peri-implantitis and/or peri-implant mucositis treatment 4. Refusal to participate in the study

Design outcomes

Primary

MeasureTime frameDescription
Bleeding on probing [positive (+) or negative (-)]About 5-10 years after surgeryWhen bleeding is present after probing using a periodontal probe with a force of 0.2-0.3 N.
Peri-implant probing depth (mm)About 5-10 years after surgeryMeasured using a periodontal probe inserted into the peri-implant sulcus
Bone loss (mm)About 5-10 years after surgeryMeasured apically from the most coronal portion of the intraosseous part of the implant using periapical radiographs

Contacts

Primary ContactXinbo Yu
xinboyu@proton.me18019409340

Outcome results

None listed

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