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NCT03841656 Clinical Trial

Influence of Gum Disease Treatment on Long-term Dental Implant Success

Periodontitis Clinical Trial

Official title:
Influence of Periodontal Care Response on Implant Treatment Outcomes at Long-term

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT03841656
Other study ID # 67RC001
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date March 1, 2019
Est. completion date March 1, 2022

Study information
Verified date February 2019
Source University Hospital, Strasbourg, France
Contact Olivier HUCK
Phone 00333
Email olivier.huck@chru-strasbourg.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of this study is to evaluate the influence of periodontal care response on long term dental implant success. Investigator's hypothesis is that patients who do not well respond to periodontal care have more chance to develop peri-implant complications at long-term. The second purpose of this study is to evaluate the influence of other local, systemic, behavioral, and implant's related risk factors

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 200
Est. completion date March 1, 2022
Est. primary completion date March 1, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria:

Patient attending supporting periodontal therapy with at least one implant placed for more than 3 years

- Patient with more than 12 teeth at baseline

- Patient with demographic, periodontal, implant data recording

- patient aged >30 years at Baseline

Exclusion criteria:

- Patient needed antibiotic prophylaxis

- Uncontrolled diabetes

- Systemic inflammatory or autoimmune diseases

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• PARORISKIMPLANT
Patients attending periodontal and implant treatment at the Department of Periodontology of the Dental Faculty at Strasbourg, France, between 2000-2015.

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
University Hospital, Strasbourg, France

Outcome
Type Measure Description Time frame Safety issue
Primary Presence of peri-implantitis as measured by probing depth The implant has a probing depth more than or equal to 4 mm At least 3 years after dental implant placement
Primary Presence of peri-implantitis as measured by erythema The implant has bleeding on probing At least 3 years after dental implant placement
Primary Presence of peri-implantitis as measured by radiographic bone loss The implant has a radiographic bone loss when compared to previous radiographs At least 3 years after dental implant placement
Secondary Implant survival presence of implant on arch Peri-implant mucositis: presence of bleeding on probing At least 3 years after dental implant placement
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