Peri-implant Disease and Prosthetic Cement: Cross-sectional Study - Trial NCT05945836
Access comprehensive clinical trial information for NCT05945836 through Pure Global AI's free database. This phase not specified trial is sponsored by University of Bologna and is currently Completed. The study focuses on Peri-implant Mucositis,Peri-Implantitis. Target enrollment is 46 participants.
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Study Focus
Observational
Sponsor & Location
University of Bologna
Timeline & Enrollment
N/A
Oct 29, 2018
Jul 19, 2019
Primary Outcome
Prevalence of submucosal cement
Summary
The main objective of the present clinical study project, of a cross-sectional observational
 nature, is to evaluate the presence of submucosal cement residues through endoscopic
 visualization in clinical situations with peri-implant disease.
 
 The secondary objective is to investigate the potential correlation between the severity of
 the pathological condition and the spatial position of cement residues in relation to the
 implant-prosthetic unit.
 
 For each subject, the following data were collected: gender, age, periodontal history,
 smoking habits, reasons for implant rehabilitation (trauma, caries, periodontitis, agenesis,
 other), the position of the implant in the oral cavity, elapsed time between prosthetic
 rehabilitation and pathological condition. If the deposit was recognized as cement residue,
 its presence was recorded, and the anatomical position of the cement residue (mesial, distal,
 lingual/palatal, vestibular) and the spatial position of cement residues in relation to the
 implant-prosthetic unit were collected.
ICD-10 Classifications
Data Source
ClinicalTrials.gov
NCT05945836
Non-Device Trial