None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Patients with missing tooth from maxillary posterior region with residual bone height lesser than 8mm and more than 4mm 2. Patients with good oral hygiene and healthy periodontal status. 3.No acute infection is present. 4.Informed and signed consent.
Exclusion criteria
Exclusion criteria: 1. Uncontrolled diabetes (HBA1c greater than 7.5%) 2.Treated or under treatment with bisphosphonate for any medical illness 3.Irradiated in the head and neck area in the last 5 years 4. Pregnant or breast feeding 5.Substance abusers 6. Psychiatric problems or unrealistic expectations 7. Patient not fully able to comply with the study protocol Local exclusion criteria consisted of the following 1.Residual bone height greater than 8mm 2. Maxillary sinus conditions contraindicating sinus floor elevation 3.Poor oral hygiene and motivation (Full Mouth Plaque Score greater than 20% and or Full Mouth Bleeding Score greater than 10%)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Endosinus bone gain: - To measure the extent of endosinus bone gain achieved in the grafted and non-grafted groups through CBCTTimepoint: 4 Months | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Bone density assessment: - To assess changes in bone density at the implant site following osseodensification in both grafted and non-grafted groups using CBCT 2. Primary stability evaluation: - to evaluate and compare the primary stability of implants placed in the sinus lift site using torque rachetTimepoint: 0 DAYS | — |
Countries
India
Contacts
Faculty of dental sciences, IMS, BHU