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Ten Years Follow up of Peri-implant Surgery

10 Years Follow-up of Patients With Residual Pockets Following the Surgical Treatment of Peri-implantitis

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04254406
Enrollment
41
Registered
2020-02-05
Start date
2019-01-01
Completion date
2019-10-01
Last updated
2020-02-05

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

Conditions

Peri-Implantitis

Keywords

Peri-Implantitis surgery, Treatment outcome, Risk factors

Brief summary

To report 10-years follow up of patients following the surgical treatment of peri-implantitis and to identify possible risk indicators for the progression of disease during supportive peri-implant therapy.

Detailed description

The data for this retrospective clinical evaluation were collected from the files and radiographs of consecutive patients who had received surgical treatment of peri-implantitis between 2007 and 2009 and thereafter enrolled in supportive peri-implant treatment (SPT) . Between 2007 and 2009, 41 patients with at least 1 implant with peri-implantitis that underwent peri-implant surgery were enrolled in a supportive peri-implant therapy. At the 2-years follow up, two groups could be identified, one responding group (17 patients) who did not present any implants with peri-implantitis and a no-responding Group (22 patients), presenting still peri-implantitis. Following the 2-years control visit, 17 patients of the responding group exited the supporting peri-implant therapy at the specialist clinic. They continued the routine controls at their referral clinics while the 22 patients of the no-responding group, continued the scheduled supportive peri-implant therapy (SPT) given at the specialist clinic.

Interventions

Evaluation of routine treatment

Sponsors

Osaka University Japan
CollaboratorUNKNOWN
Public Dental Service, Specialist Clinics, Sweden
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL

Inclusion criteria

\- All patients treated with peri-implantitis surgery between 2007 and 2009 using an anti-infective protocol.

Exclusion criteria

* Patients treated with peri-implantitis surgery between 2007 and 2009 using a regenerative protocol at one single implants with peri-implantitis.

Design outcomes

Primary

MeasureTime frameDescription
Percentage of subjects with persisting peri-implantitis10 yearsThe percentage of patients with persisting peri-implantitis following peri-implantitis surgery will be calculated among all the patients that were treated. For definition of peri-implantitis see description at outcome 1.
Number patients with persisting peri-implantitis following peri-implant surgery10 yearsThe total number of patients with persisting peri-implantitis will be calculated. Any subject presenting at least one implants with a pathological pocket will be regarded as positive for the disease . The presence or absence of peri-implantitis will be assessed by using a periodontal probe around the mucosa of the implants. The definition of a pathological pocket around an implant is a pocket of 5 millimeters or more deep with concomitants bleeding after the use of the probe.
Number of implant with persisting peri-implantitis10 yearsThe number of implants with persisting clinical signs of peri-implantitis will be calculated. Any implant presenting a pathological pockets around its surface will be regarded as positive for the disease. For definition of peri-implantitis see description at outcome 1
Percentage of implants wih persisting peri-implantitis10 yearsThe percentage of implants with persisting peri-implantitis after surgery will be calculated among all the implants that were surgically treated. For definition of peri-implantitis see description at outcome 1

Secondary

MeasureTime frameDescription
Assessement of risk factors related to the persistence of peri-implantitis10 yearsA univariate logistic regression to assess the correlations between each independent variable and the binary outcome presence or absence of peri-implantitis at treated implants will be used. Then, a multivariable regression analysis will be use including the independent variables from the univariate analysis that reach a statistical significance after adjusting for gender and age.

Countries

Sweden

Outcome results

None listed

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