Condition: Peri-Implantitis · Sponsor: Wroclaw Medical University
A total of 100 adult volunteers of both sexes will be enrolled in the project. The study will be conducted within an international consortium formed for the project, comprising the following institutions: Wroclaw Medical University (Poland), Sapienza University of Rome (Italy), University of Barcelona (Spain), University of Bern (Switzerland), and Egas Moniz University (Portugal). Each international partner institution will recruit 20 volunteers as participants in the experiment. Each of the participating institutions will submit an application to their respective local bioethics committee for approval to conduct the medical experiment. Each partner institution will conduct procedures at their respective clinical locations. Eligibility Criteria participants must have undergone previous implant treatment that has resulted in active, advanced peri-implantitis. Exclusion Criteria: General and local contraindications for surgical procedures Pregnancy; Use of bisphosphonates or other antiresorptive medications in medical history Laboratory Analysis Procedures. During the initial visit, patients will undergo a medical interview and a dental examination with regard to: Oral Hygiene Indices; Periodontal disease indices. For the implant site, the following parameters will be evaluated: Pocket Depth Bleeding on Probing Width and height of the attached gingiva Possible implant mobility, assessed using the Mobility Index Following the clinical examination, each participant will be refe…
This description comes directly from the study's public registry record.
Pawel Kubasiewicz-Ross, PhD, DDS · 504075920 · pawel.kubasiewicz-ross@umw.edu.pl
Jacek Matys, PhD, DDS · 791511789 · jacek.matys@umw.edu.pl
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| Oral Surgery Department Wroclaw Medical University | Wroclaw, Lower Silesian Voivodeship, Poland | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07012915