About this trial
The goal of this study is to investigate the clinical efficacy of different maxillary sinus floor elevation procedures based on maxillary sinus anatomy.
The main questions it aims to answer are:
* How does the anatomical morphology of maxillary sinus affect postoperative bone resorption? * How to select the appropriate maxillary sinus floor elevation procedure based on maxillary sinus anatomy? Preoperative, immediate postoperative, and six-month postoperative CBCT images of patients undergoing translateral maxillary sinus floor elevation or hydraulic transcrestal maxillary sinus floor elevation will be measured.
Eligibility criteria
Qualifiers
Patients undergoing translateral maxillary sinus floor elevation or hydraulic transcrestal maxillary sinus floor elevation in the maxillary molar region.
Patients undergoing maxillary sinus floor elevationwith simultaneous implantation in the maxillary molar region,and having successful osseointegration after 6 months from surgery.
Patients having CBCT examination for preoperative, the day of surgery, and six months after surgery.
Patients treated between January 1, 2016 and June 30, 2024.
Disqualifiers
Patients having osteointegration failure within six months after surgery.
Refusal to participate in the study.
Other conditions deemed unsuitable for participation by the investigator.
Trial design
Treatments tested in this trial
- Translateral Maxillary Sinus Floor Elevation
- Hydraulic Transcrestal Maxillary Sinus Floor Elevation