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Assessment of Early Healing Period of Dental Implants

Assessment of Volumetric Changes During the Early Healing Period of Dental Implant Treatment: Clinical, Radiographic, and Digital Evaluation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06554444
Enrollment
20
Registered
2024-08-15
Start date
2024-09-02
Completion date
2026-09-02
Last updated
2026-07-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Biological Width, Dental Implant, Osseointegration

Brief 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.

Interventions

Dental implants will be placed in edentulous areas.

Sponsors

Kutahya Health Sciences University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SCREENING
Masking
NONE

Intervention model description

Dental implant placement in the posterior mandible

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Linear and volumetric changes in the tissuePreoperative and postoperative 2nd, 4th, and 16th monthsLinear and volumetric changes in the tissue resulting from the alignment of scan data obtained at four different time points.

Secondary

MeasureTime frameDescription
Keratinized mucosa width (from the edentulous ridge)Preoperative and postoperative 2nd monthKeratinized tissue measured from the mid-buccal of the edentulous area using a periodontal probe.
Keratinized mucosa width (from the gingival margin of the dental implant-supported prosthesis)Postoperative 4th and 16th monthsKeratinized tissue measured from the gingival margin of the dental implant-supported prosthesis to the mucogingival junction using a periodontal probe.
Mucosal thickness (from the edentulous ridge)Preoperative and postoperative 2nd monthMucosal thickness measured from the midpoint of the edentulous area using a periodontal probe.
Mucosal thickness (from the facial aspect of the edentulous ridge)Preoperative and postoperative 2nd monthMucosal thickness measured at the mid-buccal of the edentulous area, from the midpoint between the mucogingival junction and 2 mm apical to the gingival margin of the adjacent tooth, using a endodontic spreader.
Mucosal thickness (from 3 mm apical to the gingival margin of the implant-supported prosthesis)Postoperative 4th and 16th monthsMucosal thickness measured 3 mm apical to the gingival margin of the implant-supported prosthesis using a endodontic spreader.
Peri-implant pocket depthPostoperative 4th and 16th monthsPeri-implant pocket depth measured at six points around the dental implant using a periodontal probe.
Modified plaque indexPostoperative 4th and 16th monthsModified plaque index measured at four points around the dental implant using a periodontal probe.
Modified bleeding indexPostoperative 4th and 16th monthsModified bleeding index measured at four points around the dental implant using a periodontal probe.
Marginal bone levelPreoperative and postoperative 2nd, 4th, and 16th monthsMarginal bone level measured on periapical radiographs.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 25, 2026