- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06128850
Peri-implant Conditions Mimic Periodontal Conditions
Peri-implant Health and Disease Mimic Periodontal Health and Disease
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.
Study Overview
Status
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
-
Bolu, Turkey
- Bolu Abant İzzet Baysal University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
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
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Peri-implantitis
|
compare to diseases
|
Peri-implant mucositis
|
compare to diseases
|
Peri-implant health
|
compare to diseases
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
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.
|
Baseline
|
Plaque index
Time Frame: Baseline
|
The plaque index assesses the amount of dental plaque visible on the vestibular and lingual surfaces of all teeth
|
Baseline
|
Gingival index
Time Frame: Baseline
|
This measurement is based on the presence or absence of bleeding on gentle probing
|
Baseline
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Periodontal pocket depth
Time Frame: Baseline
|
a pathologically deepened gingival sulcus around a tooth at the gingival margin.
|
Baseline
|
Clinical attachment level
Time Frame: Baseline
|
CAL is calculated by subtracting the gingival margin level from the probing depth.
|
Baseline
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2022/163
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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