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Vertical Augmentation Using Onlay Versus Inlay Autogenous Graft With Simultaneous Implant Placement.

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

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03052387
Enrollment
12
Registered
2017-02-14
Start date
2017-03-31
Completion date
2017-12-31
Last updated
2017-02-23

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

Conditions

Bone Resorption

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

Interventions

\* Local anesthesia with vasoconstrictor(V.C) used for hemostasis. chin block graft * Scrubbing and draping of the patient will be carried out in a standard fashion using betadine surgical scrub. * The donor site is usually the chin area, its approached using local anesthesia with VC at symphysis region. * Low vestibular incision exposing the symphysis area to the inferior border of the mandible. * Using fissure bur to harvest the graft for the defect. * Closure using vicryl 3-O sutures.

Sponsors

Cairo University
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
21 Years to 55 Years
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frameDescription
vertical Bone gain6 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

MeasureTime frameDescription
crestal bone loss6 monthscrestal bone loss around the implant will be measured in millimeter after 6 months

Outcome results

None listed

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