ClinicalTrials.gg
Active, not recruitingNCT07876687RA1-2025Updated Oct 15, 2026

Reject Analysis of Periapical Radiographs of Dental Implants.

An observational study in Healthy, sponsored by University Ghent. Active, not recruiting at 1 site in Belgium. Per ClinicalTrials.gov, last updated 2026-10-15.

Sponsored by University Ghent · Observational

Updated Oct 15, 2026Newly registeredGo to Updates ↓
Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
49
Sex
All
01

Study summary

Periapical radiographs of dental implants, acquired as part of two ongoing research projects, will be retrospectively analyzed using a newly developed image quality scoring form. Following an initial classification (Excellent - Acceptable - Rejected), a detailed assessment of the various image quality criteria and any deviations from these criteria will be performed. In addition, the frequency with which radiographs had to be retaken to obtain a diagnostically acceptable image will be evaluated. The influence of anatomical factors (e.g., implant location in the mouth, maxilla or mandible, etc.) and the use of individualized radiographic holders will also be assessed.

Through this retrospective analysis of an existing dataset of implant radiographs, the study aims to identify the factors that have influenced image quality, the ability to accurately assess the surrounding bone level, and the need for repeat radiographic exposures. The findings may contribute to the development of guidelines to improve the quality of periapical radiographs and potentially reduce radiation exposure for patients.

02

Conditions studied

  • Healthy

Keywords

  • reject analysis
  • periapical radiograph
  • dental implants
  • quality analysis
03

In context

Lead sponsor

University Ghent is the lead sponsor of 349 studies on the registry; 86 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Fourty-nine fully edentulous patients, either in the upper- and/or lower jaw being treated with a bar-retained overdenture and werd seen at the yearly evaluation after 6 to 8 years of follow-up.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

Patients which were treated with dental implants for a bar-retained overdenture in the upper - or lower jaw, as part of two running investigations.

Fully edentulous for minimally 4 months; Adequate bone volume to receive two or 4 implants

Exclusion criteria

Exclusion Criteria:

\<21 years old; Smoking

05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
49 participants (actual)
Patient registry
No

Groups and cohorts

  • Patients having received dental implants used for a bar-retained overdenture.

    Patients were treated with either 4 implants in the upper jaw or 2 implants in lower jaw as part of 2 running research projects. Periapical radiographs taken during these investigations will be analysed retrospectively .

06

What researchers measure

Primary outcomes

  1. Rejection classification

    The percentage of periapical radiographs classified as qualitatively excellent, acceptable or unacceptable.

    Time frame: Through study completion, an average of 1 year.

  2. Repeat rate

    Number of radiographs which were actually repeated as result of unacceptable quality.

    Time frame: Through study completion, an average of 1 year.

  3. Interexaminer reproducibility of the reject analysis.

    The degree of agreement between different examiners when classifying radiographs as rejected, acceptable or excellent, and when identifying the reasons for rejection according to the quality assessment criteria.

    Time frame: Through study completion, an average of 1 year.

  4. Intra-examiner reproducibility

    The degree of agreement within the different examiners when classifying radiographs as rejected, acceptable or excellent, and when identifying the reasons for rejection according to the quality assessment criteria.

    Time frame: Through study completion, an average of 1 year.

Secondary outcomes

  1. Qualitative error classification

    Frequency analysis of errors resulting in the rejection of the radiographs.

    Time frame: Through study completion, an average of 1 year.

07

Study locations

1 site
  • Oral Health Sciences - Department of Periodontology and Oral Implantology - P8
    Ghent, Oost-Vlaanderen 9000, Belgium
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References and documents

Individual participant data

Plan to share: No — Sharing individual participant data will not be relevant for analysing the quality of the publication.

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 15, 2026
Show all 1 update
  1. Oct 15, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

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Registry details

Key details

Study ID
NCT07876687
Lead sponsor
University Ghent
Responsible party
Sponsor
First posted
Oct 15, 2026
Start date
Jan 1, 2026
Primary completion
Dec 31, 2026 (estimated)
Completion
Jul 1, 2027 (estimated)
Last update
Oct 15, 2026

Study contacts

Véronique Christiaens, Prof. Dr.
principal investigator · Department of Periodontology & Oral Implantology, Faculty of Medicine and Health Sciences

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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