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
• Status: Not yet recruiting
• 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
• 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

Related Conditions & MeSH terms

• Periodontitis

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