20 subjects suffering from non restorable maxillary premolar teeth will be randomly devided into two groups. the selected teeth will be extracted and immeiate implants will be placed in all subjects. the first group will recieve deprotienized bovine bone (tutogen) to fill the buccal space between the implant and the bone, the second group will recieve platlet rich fibrin to fill the buccal space between the implant and the bone
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
20
Patient morbidity
patient pain level on pain scale using pain chart
Time frame: 14 days
crestal bone loss
radiographic analysis computing amount of crestal bone loss around implants using cone beam computed tomography
Time frame: 3 months
implants stability quotient
implant stability measured using resonance frequency analysis
Time frame: 3 months
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