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Clinical Trials/NCT03052387
NCT03052387
Unknown
Not Applicable

Assessment of Vertical Bone Augmentation Using Autogenous Onlay Versus Inlay Grafting Techniques With Simultaneous Implant Placement in the Anterior Maxillary Area on Patient's Esthetic Satisfaction : A Randomized Clinical Trial

Cairo University0 sites12 target enrollmentMarch 2017
ConditionsBone Resorption

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Bone Resorption
Sponsor
Cairo University
Enrollment
12
Primary Endpoint
vertical Bone gain
Last Updated
9 years ago

Overview

Brief Summary

Using autogenous Chin block for vertical augmentation with simultaneous implant placement at anterior maxilla region comparing between the Onlay and Inlay grafting techniques.

Detailed Description

to study the vertical augmentation with simultaneous implant placement at anterior maxillary region. * P: Patient requires implant at anterior maxillary ridge with vertical deficiency. * I:Inlay Sandwich Technique with immediate implant placement. * C:Onlay autogenous graft immediate implant placement. * O:Outcome name Measuring device Measuring unit Primary outcome: Vertical bone gain CBCT Millimeter -Secondary outcome(a): Crestal bone loss CBCT Millimeter

Registry
clinicaltrials.gov
Start Date
March 2017
End Date
December 2017
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Mohamed Ahmed Ahmed Hassan

Dentist at National research centre

Cairo University

Eligibility Criteria

Inclusion Criteria

  • \* Patients with partially edentulous anterior maxillary ridges.
  • Patients were free from any systemic disease that interferes with bone healing.
  • Absence of local pathosis at anterior maxillary area.
  • No history of any grafting procedure at the designated edentulous ridge.
  • The edentulous ridge vertical dimension was less than 10 mm measured from the alveolar crest to the nasal floor (i.e.ridge had vertical inadequacy) with normal horizontal alveolar dimension or patient with Increased Inter-Arch Space.

Exclusion Criteria

  • \* Patient with fully dentulous maxilla.
  • Pregnant females.
  • Presence of bad habits (severe bruxism, clenching).
  • Systemic diseases that may interfere with bone healing.e.g. uncontrolled Diabetes.

Outcomes

Primary Outcomes

vertical Bone gain

Time Frame: 6 months

* The nasal floor will be used as a fixed reference by adjusting the cross sectional long axis in the center of the area of interest and bisecting it (showing the buccolingual dimension). * All the patients will wear the radiographic dentures with radiopaque material (barium sulphate mixed with acrylic powder) filling the teeth at the area of interest to ensure that the calculations were taken at the same region. * On the cross sectional view of CBCT and at each proposed implant site, a line will be drawn starting from the crest of the ridge till the nasal floor. The height will be recorded preoperatively, immediately (1 week) and 6 months postoperatively.the difference between them in millimeters will be recorded.

Secondary Outcomes

  • crestal bone loss(6 months)

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