Atrophy of Edentulous Maxillary Alveolar Ridge
Conditions
Keywords
sinus augmentation,lifting
Brief summary
two groups undergo for graftless sinus lift using AMBE (antral membrane balloon elevation) through different antrostomy size with simultaneous implant placement
Detailed description
control group undergoes for graftless sinus lift using AMBE through large antrostomy with simultaneous implant placement. While, study group undergo for graftless sinus lift using AMBE through small antrostomy with simultaneous implant placement. the aim of the study is assessment the effect of antrostomy size on bone formation in graftless sinus lift with simultaneous implant placement. CBCT will be done before and after the surgery and after 6 months to assess of amount bone gain in mm. implant stability after 6 months will be determined by using Osstell. Primary outcome: amount of bone gain which will be measured by using linear measurement from CBCT. secondary outcome: stability of implant by using osstell
Interventions
maxillary sinus floor elevation by using balloon through either small or large antrostomy without using graft material with simultaneous implant placement
Sponsors
Study design
Masking description
assessment of the effect of the antrostomy size in graftless lateral maxillary sinus floor elevation using AMBE (antral membrane balloon elevation) with simultaneous implant placement
Intervention model description
assessment of the effect of the antrostomy size in graftless lateral maxillary sinus floor elevation using AMBE (antral membrane balloon elevation) with simultaneous implant placement
Eligibility
Inclusion criteria
1. Patients with atrophic maxilla and pneumatization of maxillary sinus with residual bone height from 3-6mm. 2. Both sexes 3. No intraoral soft and hard tissue pathology, 4. No systemic condition that contraindicate implant placement
Exclusion criteria
1. Sinus pathology. 2. Heavy smokers more than 20 cigarettes per day. 3. Patients with systemic disease that may affect normal healing. 4. Psychiatric problems. 5. Disorders to implant are related to history of radiation therapy to head and neck neoplasia or bone augmentation to implant site
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| amount of bone formation | after 6 months | measurement of amount of bone gained by using CBCT |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| implant stability | after 6 months | measurement of implant stability by using osstell |
Countries
Egypt