This trial is aiming to answer a question whether in Patients with severely atrophied, distal mandibular regions, the use of allogenic bone rings with simultaneous dental implants, compared to autogenous bone rings, give successful clinical and radiographic outcomes without donor site morbidity
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
28
allogenic bone ring with simultaneous dental implant placement
autogenous bone ring with simultaneous dental implant placement
change in crestal bone height
cone beam computed tomography will be used to measure bone height in millimeters
Time frame: at 6 months
graft failure
signs of graft failure will be evaluated by clinical examination
Time frame: after 1 week, 6 months and after 9 months
implant loss
signs of implant loss will be evaluated by clinical examination
Time frame: after 1 week, 6 months and after 9 months
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