Bone gain to dental implants placement Oral Health
Conditions
Interventions
The study includes 4 groups
2 groups sinus lift with simultaneous implant placement, experimental group we use T-PRF as s solo filler, control group we use allograft + xenograft
2 groups sinus lift w
Sponsors
Damascus University
Eligibility
Sex/Gender
All
Age
30 Years to 60 Years
Inclusion criteria
Inclusion criteria: 1. Good oral health 2. Have missing teeth in the premolars or molars of maxillary 3. Residual bone height between 4-6 mm for first two groups and less than 4 mm for second two groups 4. Minimum width (buccal-palatal) 6mm 5. Aged between 30-60 years
Exclusion criteria
Exclusion criteria: 1. Systematic disease(diabetes-hyperthyroidism) 2. Contraindication of surgery 3. Patient refuses treatment 4. Bad oral health
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Bone gain height is measured using CBCT imaging at baseline and 6 months 2. Bone gain volume is measured using CBCT imaging at baseline and 6 months 3. Implant stability (ISQ) is measured using MegaISQ II (RAF) at immediate implantation, 3 months, and 6 months 4. Bone density (HU) is measured using CBCT imaging at immediate post-surgery and 6 months 5. Complications (membrane perforation, sinusitis) measured using patient records | — |
Secondary
| Measure | Time frame |
|---|---|
| There are no secondary outcome measures | — |
Countries
Syria
Contacts
Public ContactZakaria Awad
Outcome results
None listed