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Clinical Trials/NCT03183336
NCT03183336
Unknown
Not Applicable

Horizontal Ridge Augmentation of the Mandible Using Interpositional Autogenous Block Grafts Versus Onlay Block Grafts; Randomized Controlled Clinical Trial

Cairo University0 sites20 target enrollmentJuly 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Horizontal Ridge Deficiency
Sponsor
Cairo University
Enrollment
20
Primary Endpoint
alveolar ridge width gained
Last Updated
8 years ago

Overview

Brief Summary

20 subjects presenting with horizontal mandibular ridge width less than 5 mm were selected and randomly divided two groups (10 in each group). the first group received interpositional block grafts (harvested from the chin and ramus) covered with Platelet-rich fibrin membrane. the second group received onlay block grafts (harvested from the chin and ramus) and covered with Platelet-rich fibrin membrane. the grafts are left for 4 months. the alveolar ridge width dimensions is then measured using radiographic analysis using cone-beam computed tomography scans

Registry
clinicaltrials.gov
Start Date
July 2016
End Date
September 2017
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Ahmed H Osman

Principle investigator

Cairo University

Eligibility Criteria

Inclusion Criteria

  • Patients of both sexes with a minimum vertical bone height above the inferior alveolar canal of 10mm in the edentulous region.
  • Patients should have ridge thickness less than 5mm measured 2mm from the alveolar crest Patients should be free from any systemic disease that may affect normal healing of bone, and predictable outcome.

Exclusion Criteria

  • Patients with any systemic disease that may affect normal bone healing. Patients with drug allergies, drug or alcohol abuse, periodontal diseases or poor oral hygiene

Outcomes

Primary Outcomes

alveolar ridge width gained

Time Frame: 4 months

radiographic analysis following ridge augmentation using Cone beam computed tomography

Secondary Outcomes

  • patient morbidity following the surgical procedure(14 days)

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