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Clinical Trial Summary

Objectives: To identify patient and implant indicators influencing the non-surgical therapeutic outcomes of peri-implantitis at 6-months follow-up. Material and methods: This prospective cohort study included patients with at least one implant diagnosed with peri-implantitis according to the 2017 World Workshop. Non-surgical therapy consisted in a mechanical debridement of the peri-implant pockets combined with the metronidazole 500 mg every 8 hours during 7 days. At baseline and at 6 months, clinical and radiographic variables were collected to calculate the success of the therapy. The influence of patient and implant/prosthetic variables on disease resolution were assessed trough simple and multiple logistic regression analysis at patient and implant level using generalized estimation equations models.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05539755
Study type Interventional
Source Universitat Internacional de Catalunya
Contact
Status Completed
Phase N/A
Start date January 1, 2021
Completion date July 12, 2022

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