Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
54 participants
OBSERVATIONAL
2023-11-01
2024-05-15
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Does PPI use affect the survival rate of dental implants? Does PPI use influence crestal bone loss and fractal dimension (FD) of the surrounding bone?
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Evaluation of Fractalkine and Its Receptor in Peri-implantitis
NCT06685523
Assessment of Osseointegration Properties of Nano-Hydroxy Apatite Coated Titanium Implant
NCT05936775
Retrospective Evaluation of Prosthetic Complications and Peri-implant Bone Resorption in Implant-supported Single Unit Fixed Restorations
NCT06709508
The Impact of Anti-Resorptive Agents on Dental Implant Success
NCT07150351
Comparison of Short and Standard Dental Implants
NCT04475406
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_CONTROL
RETROSPECTIVE
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Having a history of PPI use for more than six months,
* Having at least one bone-level and axially placed dental implant in the maxilla or mandible,
* Having a minimum of one year elapsed since the prosthetic restoration following dental implant placement,
* Having undergone routine clinical follow-ups and radiological evaluations with periapical radiographs taken using the parallel cone technique after dental implant placement.
Exclusion Criteria
* Individuals with periapical radiographs of low image quality or with artifacts,
* Individuals for whom the regions selected for fractal analysis on periapical radiographs are not appropriately sized,
* Individuals who have not undergone routine clinical and radiographic follow-ups.
18 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Berkay Tokuç
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Berkay Tokuç
Associate Professor
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Kocaeli University
Kocaeli, , Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
2023/295
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.