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Peri-implant Conditions Mimic Periodontal Conditions

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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06128850
Enrollment
143
Registered
2023-11-13
Start date
2022-07-04
Completion date
2023-03-31
Last updated
2024-07-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gingivitis, Peri-implant Health, Peri-Implantitis, Peri-implant Mucositis, Periodontitis

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.

Interventions

OTHERdisease

compare to diseases

Sponsors

Abant Izzet Baysal University
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
Yes

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

* Bruxism * Uncontrolled medical conditions

Design outcomes

Primary

MeasureTime frameDescription
Plaque indexBaselineThe plaque index assesses the amount of dental plaque visible on the vestibular and lingual surfaces of all teeth
Gingival indexBaselineThis measurement is based on the presence or absence of bleeding on gentle probing
Bleeding on probingBaselineBleeding, 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.

Secondary

MeasureTime frameDescription
Periodontal pocket depthBaselinea pathologically deepened gingival sulcus around a tooth at the gingival margin.
Clinical attachment levelBaselineCAL is calculated by subtracting the gingival margin level from the probing depth.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026