Psychometric Validation of the Portuguese DIVAS-Q in Women With Vulvovaginal Atrophic Symptoms
NCT07250490
Dyspareunia, Female Urogenital Diseases
Lisbon, Lisbon District, Portugal
View Trial DetailsNCT Number: NCT02671812
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
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Notify Me20 year–81 year
All sexes
Observational
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: 10 years after implant treatment
Questionnaire and clinical examination
Time frame: 10 years after implant treatment
Self reported and registered in patients journal and detected at the clinical examination
Time frame: 10 years after implant treatment
Samples of saliva and gingival fluid from healthy and disease sites at both tooth and dental implants will be analyzed
Folktandvården Stockholms län AB
Other Gov
Longterm Outcome After Dental Implant Treatment
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