Health Condition 1: K084- Partial loss of teeth
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Adequate bone height and width after extraction to accommodate the implant without impinging on vital structures in either maxillary or mandibular arches. 2. Bone density range between =150 measured in Hounsefield units based on CBCT findings (corresponding to D3 -D4 bone density according to bone density classification by Misch). 3. Medically fit participants of age range between 24 â?? 50 years. 4. Willingness to participate for the duration of the study. 5. General good health 6. Patient who will give positive informed consent. 7. Both the edentulous areas having antagonist teeth.
Exclusion criteria
Exclusion criteria: 1. High bone density (more than 850 HU corresponding to D1and D2 level of bone density classification by Misch), 2. Bone metabolic disorders such as osteoporosis, osteomalacia, rickets affecting surrounding bone health. 3. History of radiotherapy in head and neck region. 4. Current habit of smoking or alcohol or drug abuse. 5. Systemic conditions as uncontrolled diabetic and hypertensive patients and cardiovascular conditions affecting the integrity of implant or connective tissue health surrounding the implant. 6. Bleeding dyscrasias or under anticoagulant therapy. 7. Needed augmentation of the implant site. 8. Signs of infection in the prospective implant site. 9. History of participants undertaking systemic corticosteroids, bisphosphonates or any other medications that would compromise postoperative healing or osseointegration. 10. Pregnancy / lactating mothers at the time of enrollment. 11. Parafunctional habits such as bruxism and clenching, 12. Local limitations such as inadequate inter-ridge distance 13. Poor oral hygiene and motivation 14. Untreated generalized periodontitis. 15. Full mouth plaque and the bleeding score of 15 % or less.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Comparison of bone density between osseodensification and conventional drilling techniqueTimepoint: Preoperative , Postoperative (Immediately after implant placement) and in a period of 12 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| Comparison of Implant stability between osseodensification and conventional drilling techniqueTimepoint: Postoperatively , 6 and 12 weeks after implant placement | — |
Countries
India
Contacts
AIIMS , New Delhi