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Dental ImplantEarly Bone LosNCT07625813

Early Bone Loss in Dental Implants

An observational study of Dental Implant and Marginal Bone Loss, run by Abant Izzet Baysal University at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This retrospective observational study aims to evaluate early marginal bone loss around dental implants using panoramic radiographs. Radiographic records of patients who underwent mandibular dental implant surgery and implant-supported prosthetic rehabilitation will be reviewed. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
Dental Implant, Marginal Bone Loss
How many people
256 participants
Where
1 siteTurkey (Türkiye)
Study dates
15 Jan 2025to 15 Feb 2026
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Study population: The study population will consist of adult systemically healthy patients who underwent mandibular dental implant surgery and implant-supported prosthetic rehabilitation at Bolu Abant Izzet Baysal University Faculty of Dentistry between 2012 and 2025 and had suitable panoramic radiographs available for retrospective radiographic evaluation of marginal bone loss.

Who may be able to join

  • Individuals older than 18 years
  • Patients with mandibular dental implants
  • Availability of panoramic radiographs obtained after implant surgery and after prosthetic loading
  • Panoramic radiographs suitable for radiographic evaluation
  • Visibility of the mandibular inferior cortex and mental foramen on panoramic radiographs
  • Systemically healthy individuals

Who cannot join

  • Low-quality panoramic radiographs
  • Missing follow-up radiographs
  • Presence of systemic diseases or conditions that may affect bone metabolism

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Faculty of Dentistry, Bolu Abant İzzet Baysal University, Department of Periodontics

    Bolu, Central, 14100

Other trials in Turkey (Türkiye)

About this study

Official title: Retrospective Evaluation of Early Bone Loss in Dental Implants

This retrospective observational study aims to evaluate early marginal bone loss around dental implants using panoramic radiographs. Radiographic records of patients who underwent mandibular dental implant surgery and implant-supported prosthetic rehabilitation will be reviewed. Marginal bone loss will be measured on the mesial and distal aspects of each implant at final restoration delivery and at follow-up periods after prosthetic loading. The study will also assess patient-, implant-, and prosthesis-related factors associated with marginal bone loss.

Keywords
Dental implants, Early bone loss, Marginal bone loss, Peri-implant bone loss, Implant-supported prosthesis
Medical subject headings
Bone Diseases, Metabolic

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT07625813
Study groupRoleWhat they receive
Dental Implant PatientsPatients with mandibular dental implants who had suitable panoramic radiographs for retrospective evaluation of marginal bone loss.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in Marginal Bone Loss Over Time

    Marginal bone loss will be assessed on panoramic radiographs by measuring the linear distance from the implant platform to the nearest supporting crestal bone on the mesial and distal aspects of each implant. Mesial, distal, and mean marginal bone loss values will be recorded in millimeters.

    Measured: At final restoration delivery, 6 months, 18 months, and 60 months after prosthetic loading

Secondary outcomes (9)
  1. Effect of implant length on mean marginal bone loss

    The effect of implant length on mean marginal bone loss will be evaluated using regression analysis. Implant length will be recorded in millimeters from patient records and implant system information. Mean marginal bone loss will be calculated by averaging mesial and distal marginal bone loss measurements for each implant.

    Measured: Up to 60 months after prosthetic loading

  2. Effect of implant diameter on mean marginal bone loss

    The effect of implant diameter on mean marginal bone loss will be evaluated using regression analysis. Implant diameter will be recorded in millimeters from patient records and implant system information. Mean marginal bone loss will be calculated by averaging mesial and distal marginal bone loss measurements for each implant.

    Measured: Up to 60 months after prosthetic loading.

  3. Effect of abutment height on mean marginal bone loss

    The effect of abutment height on mean marginal bone loss will be evaluated using regression analysis. Abutment height will be recorded in millimeters from prosthetic records. Mean marginal bone loss will be calculated by averaging mesial and distal marginal bone loss measurements for each implant.

    Measured: Up to 60 months after prosthetic loading.

  4. Effect of implant-tooth distance on mean marginal bone loss

    The effect of implant-tooth distance on mean marginal bone loss will be evaluated using regression analysis. Implant-tooth distance will be measured on panoramic radiographs as the horizontal distance between the implant and the adjacent natural tooth when applicable. Mean marginal bone loss will be calculated by averaging mesial and distal marginal bone loss measurements for each implant.

    Measured: Up to 60 months after prosthetic loading.

  5. Effect of implant-implant distance on mean marginal bone loss

    The effect of implant-implant distance on mean marginal bone loss will be evaluated using regression analysis. Implant-implant distance will be measured on panoramic radiographs as the horizontal distance between adjacent implants when applicable. Mean marginal bone loss will be calculated by averaging mesial and distal marginal bone loss measurements for each implant.

    Measured: Up to 60 months after prosthetic loading.

  6. Effect of emergence profile angle on mean marginal bone loss

    The effect of emergence profile angle on mean marginal bone loss will be evaluated using regression analysis. Emergence profile angle will be recorded in degrees when applicable. Mean marginal bone loss will be calculated by averaging mesial and distal marginal bone loss measurements for each implant.

    Measured: Up to 60 months after prosthetic loading.

  7. Mean marginal bone loss according to implant placement level

    Mean marginal bone loss will be compared according to implant placement level. Implant placement level will be categorized as crestal, subcrestal, or supracrestal according to the vertical position of the implant platform relative to the crestal bone level. Mean marginal bone loss will be calculated by averaging mesial and distal marginal bone loss measurements for each implant.

    Measured: Up to 60 months after prosthetic loading.

  8. Mean marginal bone loss according to prosthetic restoration type

    Mean marginal bone loss will be compared according to prosthetic restoration type. Prosthetic restoration type will be categorized according to the type of implant-supported prosthetic rehabilitation, including single crown, fixed partial prosthesis, splinted crowns, full-arch fixed restoration, or removable prosthesis. Mean marginal bone loss will be calculated by averaging mesial and distal marginal bone loss measurements for each implant.

    Measured: Up to 60 months after prosthetic loading.

  9. Mean marginal bone loss according to opposing arch condition

    Mean marginal bone loss will be compared according to opposing arch condition. Opposing arch condition will be categorized according to the dentition or prosthetic status of the opposing arch. Mean marginal bone loss will be calculated by averaging mesial and distal marginal bone loss measurements for each implant.

    Measured: Up to 60 months after prosthetic loading.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted4 Jun 2026
  2. Study start15 Jan 2025
  3. Primary completion15 Jan 2026
  4. Study completion15 Feb 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Retrospective
Enrolment
256 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07625813
Sponsor's protocol ID
BAİBU-Perio-ZA-03
Acronym
Early Bone Los
Status last verified
Jun 2026
First submitted
23 May 2026
Last updated
4 Jun 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Dental Implant and Marginal Bone Loss, run by Abant Izzet Baysal University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 4 Jun 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in Marginal Bone Loss Over Time (time frame: At final restoration delivery, 6 months, 18 months, and 60 months after prosthetic loading). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 Jun 2026.

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Early Bone Loss in Dental Implants (NCT07625813) | AzTrials