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Horizontal Ridge Augmentation of the Mandible Autogenous Block Grafts

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

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03183336
Enrollment
20
Registered
2017-06-12
Start date
2016-07-31
Completion date
2017-09-30
Last updated
2017-07-11

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

Conditions

Block Graft, Horizontal Ridge Deficiency

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

Interventions

PROCEDUREridge split interpositional block graft
PROCEDUREdecortication Onlay block graft

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

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

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

Design outcomes

Primary

MeasureTime frameDescription
alveolar ridge width gained4 monthsradiographic analysis following ridge augmentation using Cone beam computed tomography

Secondary

MeasureTime frameDescription
patient morbidity following the surgical procedure14 dayspain value on pain scale

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026