NCT05945836

Peri-implant Disease and Prosthetic Cement: Cross-sectional Study

Excess Cement and Peri-implant Disease: A Cross-sectional Clinical Endoscopic Study
University of Bologna·ClinicalTrials.govCompleted
View on ClinicalTrials.gov
Study focus
Study type
Observational
Sponsor & location
Primary sponsor
University of Bologna
Location
Bologna, Italy
Timeline & enrollment
Phase
N/A
Start date
Oct 29, 2018
End date
Jul 19, 2019
Enrollment
46 participants
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
Oral mucositis (ulcerative)Infection and inflammatory reaction due to other internal orthopaedic prosthetic devices, implants and graftsInfection and inflammatory reaction due to prosthetic device, implant and graft in genital tractInfection and inflammatory reaction due to other internal prosthetic devices, implants and graftsPeritonitis
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT05945836
Type
Non-Device Trial
About this record

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.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.