Prevalence and Risk Indicators of Peri-implant Diseases in China

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

NOT_YET_RECRUITING

Total Enrollment

500 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-01-31

Study Completion Date

2025-01-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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.

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Evaluation of the Prevalence and Risk Factors for Patients With Peri-implant Disease：a Retrospective Study

NCT02662361

Jaw, Edentulous, Partially

UNKNOWN

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

NCT02676661

Jaw, Edentulous, Partially

UNKNOWN

Evaluation of the Related Factors Influencing the Stability of Dental Implants

NCT02733861

Teeth Missing

UNKNOWN

Impact of Buccal Bone Thickness on Pathological Peri-implant Bone Loss: A 3-year Prospective Cohort Study

NCT02939222

Periimplantitis Oral Surgery

WITHDRAWN NA

Clinical Outcomes of Resective Surgical Treatment of Peri-Implantitis With or Without Implantoplasty

NCT04259840

Peri-Implantitis

TERMINATED

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Peri-Implantitis

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

ECOLOGIC_OR_COMMUNITY

Study Time Perspective

CROSS_SECTIONAL

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Patients

Patients having at least one rough surface titanium implant in function for more than 5 years.

No interventions assigned to this group

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No