Skip to main content
Clinical Trials/NCT02671812
NCT02671812
Completed
N/A

Longterm Outcome After Dental Implant Treatment

Folktandvården Stockholms län AB0 sites163 target enrollmentNovember 27, 2014

Overview

Phase
N/A
Intervention
Not specified
Conditions
PROMs
Sponsor
Folktandvården Stockholms län AB
Enrollment
163
Primary Endpoint
Patients satisfaction after dental implant treatment
Status
Completed
Last Updated
3 months ago

Overview

Brief Summary

The general aim of this project is to investigate the long-term treatment outcome after implant therapy. The patients' satisfaction with implant treatment will be studied and correlated to biological and technical problems. The survival rates of implants at patient level and the degree of bone loss of remaining teeth and implants will be calculated. The levels of cytokines and bone loss markers in peri-implantitis sites and periodontal defects and at healthy sites will be analyzed in order to study the correlation between cytokine and bone loss marker levels, and clinical conditions. Independent variables which could be regarded as significant risk factors or risk predictors on the incidence of peri-implantitis are aimed to be identified

Detailed Description

* A questionnaire study will investigate patient satisfaction 8-14 years after dental implant therapy to study if complications influence the degree of satisfaction/quality of life. The questionnaire will be sent to 587 patients treated at The Specialist Clinic Skanstull. * A clinical examination of a minimum 150 patients who answered the questionnaire will be performed: * to study the incidence of biological and technical complications on dental implants after a minimum of 10 year of function. * to study the survival rates of implants at patient level and the degree of bone loss of remaining teeth and implants. In addition, the correlation between bone loss of remaining teeth and bone loss of implants will be studied. * samples taken from the gingival crevicular fluid to investigate the profile of cytokines and bone resorption markers as well as to study the intra-individual correlation of cytokines and bone markers in gingival crevicular fluid from sites with peri-implantitis and periodontal defects in individuals with dental implants. * in addition, the salivary cytokine and bone resorption markers will be analyzed in order to identify disease-specific biomarkers as well as to study the correlation between the cytokine/bone resorption markers in saliva and in gingival/peri-implant crevicular fluid. * To identify significant risk factors or risk predictors on the incidence of peri-implantitis.

Registry
clinicaltrials.gov
Start Date
November 27, 2014
End Date
August 1, 2018
Last Updated
3 months ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Leif Jansson

DDS PhD-student

Folktandvården Stockholms län AB

Eligibility Criteria

Inclusion Criteria

  • \- Treated at the Specialist Clinic Skanstull, Stockholm, Sweden with dental implants between the years of 1999-2005

Exclusion Criteria

  • \- Deceased before or during the study period

Outcomes

Primary Outcomes

Patients satisfaction after dental implant treatment

Time Frame: 10 years after implant treatment

Questionnaire and clinical examination

Secondary Outcomes

  • Complications prevalence(10 years after implant treatment)
  • Profile of inflamatory markers(10 years after implant treatment)

Similar Trials