Dental Implant Surgery: Dental implants will be placed in edentulous areas.
Study summary
This prospective cohort study aimed to evaluate, clinically, radiographically, and digitally, the volumetric changes occurring during the early healing period after implant treatment in patients with tooth loss in the posterior regions of the jaws, focusing on the processes of osseointegration and biological width formation.
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria:
* Over the age of 18
* Systemically healthy
* Need for implant treatment in unilaterally edentulous posterior mandible
* Sufficient interocclusal space for implant and restoration placement
* At least four months passed since tooth extraction
* Alveolar bone height adequate for implant placement, with a minimum width of 6 mm, and without risking anatomical structures
* Plaque and bleeding scores of less than 15% in the entire mouth
* Presence of opposing teeth in occlusion
* Written informed consent obtained, including permission for the use of data for research purposes
Exclusion Criteria:
* Poor oral hygiene
* Uncontrolled periodontal disease
* Pregnancy or lactation at any stage of the study
* Uncontrolled diabetes
* Patients with suppressed immune systems
* History of radiotherapy to the head and neck region
* Diseases or medications affecting bone metabolism
* Smoking more than 10 cigarettes per day
* Bone augmentation performed before or concurrently with the implant
* Failure to achieve primary stability with the implant
Primary outcome measure(s)
Linear and volumetric changes in the tissue — Preoperative and postoperative 2nd, 4th, and 16th months Linear and volumetric changes in the tissue resulting from the alignment of scan data obtained at four different time points.
Trial sites (1)
Facility
City
Region
Status
Kutahya Health Sciences University
Kütahya
Turkey (Türkiye)
More Kutahya Health Sciences University trials in Turkey
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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