Osseointegration of posterior implants.
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients should have sufficient bone volume for implant placement without GBR (Guided Bone Regeneration) Patients should have signed an informed consent form The target bone should be type D3 or D4. Patient cooperation should be excellent
Exclusion criteria
Exclusion criteria: Patients with insufficient bone volume requiring GBR Bone type D1 or D2 Need for implants in areas other than mandibular premolars and molars Need for implants only on one side of the mandible (inability to perform split-mouth design) Systemic diseases affecting bone healing process Use of medications affecting bone metabolism History of radiotherapy in the head and neck region
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Implant stability measured by Ostell device on days 0, 10, 21, and 42 post-surgery. Timepoint: On days 0, 10, 21, and 42 post-surgery. Method of measurement: Implant stability measured by Ostell device. | — |
Countries
Iran (Islamic Republic of)
Contacts
Mashhad University of Medical Sciences