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A Clinical Investigation to Evaluate the Healing of Tooth Extraction Sites Filled With BioRestore™

Phase 1
Completed
Conditions
Alveolar Bone Loss
Interventions
Device: Alveolar Bone Defect Regeneration Following Tooth Extraction
Registration Number
NCT01105026
Lead Sponsor
University of Trieste
Brief Summary

The aim of this study was to evaluate by histology and MSCT scans during a 7-month period, the efficacy of a bioactive glass (Inion BioRestore™) placed in human extraction sockets in the maintenance of alveolar ridge.

Detailed Description

14 subjects in need of implant therapy were enrolled in the study. A total of 32 teeth were extracted and the fresh sockets underwent to ridge preservation procedures using Inion BioRestore™. Two different time points (1 week and 3 months after RPP) MSCT scans for each patient were used as a basis for bone change analysis occurred in the localized grafted alveolar sites. Twenty-two biopsied, representative of intermediate (3-4 months, n=10) and late phase (6-7 months, n=12) of healing, were harvested and histologically analysed.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
14
Inclusion Criteria
  • Systemically healthy females or males subjects.
  • They did not smoke
  • Did not take any medications.
Exclusion Criteria
  • Subjects with less than 18 years of age,
  • with current alcohol or drug abuse,
  • with systemic/local conditions that would interfere with wound healing or osseointegration
  • with a history of chemotherapy and radiotherapy in the head and neck region.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
bioactive glassAlveolar Bone Defect Regeneration Following Tooth Extraction-
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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