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The Influence of Cortical Bone Perforation on Guided Bone Regeneration in Humans

M

Mashhad University of Medical Sciences

Status

Completed

Conditions

Alveolar Bone Loss

Treatments

Procedure: Decortication

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The purpose of this randomized clinical trial was to evaluate the effect of cortical bone decortication on the angiogenesis and osteogenesis of augmented ridge by GBR.

Full description

Background: The purpose of the current study was to evaluate the effect of cortical bone perforation on angiogenesis and osteogenesis of augmented ridge by guided bone regeneration.

Methods: Fourteen patients (mean age: 52) who were in need of dental implants at areas with osseous defects in the mandible were selected. In the test group (n=7), alveolar cortical bone at the area of regeneration was perforated using a #2 high speed round bur. No decortication of cortical bone was performed in the control group (n=7). Subsequently, defects were augmented by guided bone regeneration using resorbable membrane and bovine bone. After a healing period of 7 months, implant sites were created and trephine cores harvested for histological and histomorphometric analysis of the grafted areas.

Enrollment

14 patients

Sex

All

Ages

25 to 72 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Inclusion criteria were presence of atrophic mandibular ridges with bucco-lingual width ranging between 2-5 mm, as measured on serial sections of a computerized axial tomography (CAT) scan.

Exclusion criteria

  • Exclusion criteria included patients with diabetes, osteoporosis or other metabolic disorders, smokers, pregnant patients and patients who had any systemic or local factors that would inhibit normal wound healing process.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

14 participants in 2 patient groups

test group
Experimental group
Description:
decortication group
Treatment:
Procedure: Decortication
control
No Intervention group
Description:
without decortication

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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