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

U

University of Bologna

Status

Completed

Conditions

Peri-implant Mucositis
Peri-Implantitis

Study type

Observational

Funder types

Other

Identifiers

NCT05945836
peri-implant/cement

Details and patient eligibility

About

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.

Enrollment

46 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • at least one single-implant with cemented restoration and clinical-radiographic signs of peri-implant disease
  • patients with previous periodontitis had to have a healthy but reduced periodontium

Exclusion criteria

  • neuromotor pathologies or morphological-dysfunctional alterations

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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