- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07295743
Effect of Emergence Angle on Peri-implant Status (EEAPS)
December 8, 2025 updated by: Tuğba ŞAHİN, Abant Izzet Baysal University
The Effect of Implant Prosthesis Emergence Angle on Peri-Implant Health and Disease
The study was conducted at the Division of Periodontology, Bolu Abant İzzet Baysal University Faculty of Dentistry.
Participants were systemically healthy individuals aged 18 to 70 who had received dental implant prostheses within the past five years and had high-quality panoramic radiographs.
The peri-implant status of the subjects was evaluated using various indices and radiographic analyses in accordance with Chicago's Classification of Periodontal and Peri-Implant Diseases and Conditions.
Additionally, measurements of gingival thickness, gingival phenotype, keratinized gingival width, and emergence angle were performed.
Study Overview
Status
Completed
Intervention / Treatment
Detailed Description
Patient histories were collected from those who met the study criteria, and panoramic radiographs were taken.
A total of 310 implants were initially assessed, and 192 implants were selected for inclusion in the study.
All implant patients underwent an evaluation of plaque index , gingival index, bleeding on probing , pocket depth, clinical attachment level, and gingival recession.
The peri-implant condition was determined using these indices and radiographs, in accordance with the guidelines from the 2017 World Workshop on the Classification of Periodontal and Peri-Implant Diseases and Conditions and the 2023 European Federation of Periodontology.
Patients were categorized into three groups: peri-implantitis (64), peri-implant health (64), and peri-implant mucositis (64).
Additionally, gingival thickness (GT), keratinized gingival width (KGW), and gingival phenotype (GP) around the implants were measured, and the emergence angle (EA) of the implants was calculated.
Study Type
Observational
Enrollment (Actual)
192
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Bolu, Turkey (Türkiye), 14030
- Bolu Abant Izzet Baysal University, Dentistry Faculty
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
Patients who have received implants
Description
Inclusion Criteria:
- Systemically healthy individuals or individuals with controlled medical conditions
- Availability of high-quality panoramic radiographs that could be accurately measured after fabrication of the dental implant prosthesis
- Implants placed no more than five years prior to evaluation
Exclusion Criteria:
- Individuals with uncontrolled systemic diseases
- Presence of habitual bruxism
- Current smokers
- Pregnant or breastfeeding individuals
- Use of anti-inflammatory or immunosuppressive medications affecting the mucosa or bone
- Individuals who had received treatment for peri-implant disease after implant placement
- Development of peri-implantitis due to residual cement or prosthesis design, or improperly positioned implants
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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Peri-implantitis
Peri-implantitis patients are those who have developed inflammation around a dental implant, leading to the loss of supporting bone and the presence of pockets of infection.
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The emergence angles of the implants were measured on panoramic radiographs.
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Peri-implant mucositis
Peri-implant mucositis refers to a reversible inflammatory condition affecting the soft tissues surrounding a dental implant, characterized by redness, swelling, and bleeding on probing, without any bone loss.
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The emergence angles of the implants were measured on panoramic radiographs.
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Peri-implant health
Peri-implant health refers to the condition where the tissues surrounding a dental implant are free from inflammation, with no signs of redness, swelling, bleeding on probing, or bone loss, indicating a stable and healthy implant environment.
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The emergence angles of the implants were measured on panoramic radiographs.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Emergence angle
Time Frame: Baseline
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EA was determined by measuring the angle formed between the long axis of the implant and a tangent line drawn to the restoration.
A line was initially drawn along the long axis of the implant at its outside collar.
Subsequently, a second line, tangent to the restoration, was drawn from the platform.
The angle at which the junction occurred was recorded as the EA .
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Baseline
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
periodontal pocket depth
Time Frame: Baseline
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The periodontal pocket depth is the measurement of the distance between the gingival margin and the most coronal region of the junctional epithelium.
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Baseline
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bleeding on probing
Time Frame: Baseline
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The bleeding on probing index was established as the occurrence of bleeding in the sulcus, thirty seconds after measuring the depth of the periodontal pockets in all dental implant.
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Baseline
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plaque index
Time Frame: Baseline
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an index for estimating the status of oral hygiene by measuring dental plaque that occurs in the areas adjacent to the gingival margin.
0 is minimum and 3 is maximum.
The situation worsens as the score increases.
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Baseline
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gingival index
Time Frame: Baseline
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The Gingival Index (GI) scores each site on a 0 to 3 scale, with 0 being normal and 3 being severe inflammation characterized by edema, redness, swelling, and spontaneous bleeding.
0 is minimum and 3 is maximum.
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Baseline
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clinical attachment level
Time Frame: Baseline
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The peri-implant clinical attachment level is determined by measuring the distance from the implant margin to the base of the mucosal sulcus using a Williams periodontal probe.
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Baseline
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Gingival recession
Time Frame: Baseline
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Gingival recession is the measured distance between the enamel-cementum and the gingival margin.
Assessment was performed using a Williams periodontal probe.
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Baseline
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gingival thickness
Time Frame: Baseline
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GT was measured by inserting a number eight canal file from the buccal side of the implant until it reached the alveolar bone and then securing it with a stopper to determine the distance.
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Baseline
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keratinized tissue width
Time Frame: Baseline
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The width of the keratinized gingiva was measured via a periodontal probe from the mucogingival margin to the gingival margin.
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Baseline
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Tuğba Şahin, Bolu Abant İzzet Baysal Üniversity
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
September 7, 2024
Primary Completion (Actual)
April 30, 2025
Study Completion (Actual)
May 1, 2025
Study Registration Dates
First Submitted
November 18, 2025
First Submitted That Met QC Criteria
December 8, 2025
First Posted (Actual)
December 22, 2025
Study Record Updates
Last Update Posted (Actual)
December 22, 2025
Last Update Submitted That Met QC Criteria
December 8, 2025
Last Verified
December 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- AIBU-DH-TS-04
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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