Comparison of bone density and implant stability between osseodensification and conventional drilling technique â?? A split mouth randomised Controlled Trial.

A R Sanofar0 个研究点目标入组 0 人开始时间: 待定最近更新: 2023年2月6日

试验速览

暂无简介。

•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 <=850 and >=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.

•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.

发起方

A R Sanofar