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

NCT05945836 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 46

Last updated 2023-07-19

No results posted yet for this study

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.

Conditions

  • Peri-implant Mucositis
  • Peri-Implantitis

Sponsors & Collaborators

  • University of Bologna

    lead OTHER

Principal Investigators

  • Marco Montevecchi, DDS · Alma Mater Studiorum - University of Bologna

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-10-29
Primary Completion
2019-07-19
Completion
2019-07-19

Countries

  • Italy

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05945836 on ClinicalTrials.gov