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Clinical and Radiographic Outcomes of Alveolar Ridge Preservation

NCT07427784 · tracked via the Priya Life Science Italy tracker
Phase
Observational
Started
2026-03-01
Last updated
2026-03-20

Condition(s) studied

Alveolar Ridge Preservation

Study summary

Dental implants are considered a predictable rehabilitative option following tooth extraction or in cases of missing teeth. In some situations, the inevitable alveolar ridge resorption that occurs after extraction may make the placement of standard-diameter (\>3.5 mm) or standard-length implants difficult or even impossible without advanced bone augmentation procedures. To counteract post-extraction volumetric bone contraction, alveolar ridge preservation can be performed, consisting of placing a bone graft within the socket walls immediately after tooth extraction. Although this procedure cannot completely prevent dimensional changes, it has been shown to significantly reduce both horizontal and vertical ridge resorption, as reported in the scientific literature. However, there is a lack of clinical and radiographic studies evaluating the outcomes of implant rehabilitation following alveolar ridge preservation with standard-dimension implants in a hospital-based setting.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients requiring alveolar ridge preservation procedures prior to implant rehabilitation of edentulous sites; * Age \> 18; * Achievement of FMPS and FMBS ≤ 15%; * Signed written informed consent to participate in the study. Exclusion Criteria: * Uncontrolled diabetes or hypertension; * Uncontrolled periodontal disease; * Inability to perform consistent and continuous follow-up; * Pregnancy or breastfeeding; * Inability to provide written informed consent.

Primary outcome measure(s)

  • Volumetric analysis — From tooth extraction to 6 months of follow up.
    The dimensional change of hard tissues following bone regenerative procedures will be assessed radiographically by measuring horizontal and vertical bone resorption through CBCT comparison in patients treated in a hospital-based setting.

Trial sites (1)

FacilityCityRegionStatus
Catholic University of the Sacred Heart Roma Italy
Official registry record

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.

View NCT07427784 on ClinicalTrials.gov ↗ ← All trials in Italy