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Clinical Trials/NCT06128850
NCT06128850
Completed
N/A

Examining Peri-İmplant and Periodontal Conditions Co-occur: A Cross-Sectional Study

Abant Izzet Baysal University1 site in 1 country143 target enrollmentJuly 4, 2022

Overview

Phase
N/A
Intervention
Not specified
Conditions
Peri-Implantitis
Sponsor
Abant Izzet Baysal University
Enrollment
143
Locations
1
Primary Endpoint
Plaque index
Status
Completed
Last Updated
last year

Overview

Brief Summary

Except for patients with referred clinical bruxism and uncontrolled medical conditions, the study included 123 implants with implanted fixed prostheses that had lasted at least six months after functional prosthetic loading. In all implant patients, the health scale ranged from implants and natural teeth to plaque, gingival index, bleeding in the probe, mouth depth, loss of clinical attachment, and dental implants. The health and illness of the implants have been determined. Patients were divided into three groups: peri-implantitis, peri-implant mucositis, and peri-implant health.

Inclusion Criteria:

  • Patients between the ages of 18- 70
  • Drugs that have a systemically healthy and controlled treatment situation
  • Drivers who have implant-supported fixed prostheses that have been at least six months after functional prosthetic loading Among these groups, it was checked whether periodontitis was seen in patients with peri-implantitis, gingivitis in patients with peri-implant mucositis, and whether healthy gums were seen in individuals with peri-implant health.

To determine the health and disease status of individuals' implants, plaque index (Silness Loe 1964), gingival index (Loe Silness 1963), bleeding on probing (Ainoma Bay 1975), pocket depth measurements, and clinical attachment level were collected.

Registry
clinicaltrials.gov
Start Date
July 4, 2022
End Date
March 31, 2023
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Tuğba ŞAHİN

Assistant professor

Abant Izzet Baysal University

Eligibility Criteria

Inclusion Criteria

  • Patients between the ages of 18- 70
  • Drugs that have a systemically healthy and controlled treatment situation
  • Drivers who have implant-supported fixed prostheses that have been at least six months after functional prosthetic loading

Exclusion Criteria

  • Uncontrolled medical conditions

Outcomes

Primary Outcomes

Plaque index

Time Frame: Baseline

The plaque index assesses the amount of dental plaque visible on the vestibular and lingual surfaces of all teeth

Bleeding on probing

Time Frame: Baseline

Bleeding, leading sign of inflammation inside the connective tissue, is a critical factor for pocket depth measurements, and with other variable factors prevents making reproducible measurements.

Gingival index

Time Frame: Baseline

This measurement is based on the presence or absence of bleeding on gentle probing

Secondary Outcomes

  • Periodontal pocket depth(Baseline)
  • Clinical attachment level(Baseline)

Study Sites (1)

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