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
This trial does not accept healthy volunteersQualifiers
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 population
Patients undergoing maxillary sinus floor elevation with simultaneous implantation in the maxillary molar region, and having successful osseointegration after 6 months from surgery.
Trial design
Cohort
Retrospective
Treatments tested in this trial
Translateral Maxillary Sinus Floor Elevation
Procedure/SurgeryTranslateral maxillary sinus floor elevation with simultaneous implantation in the maxillary molar region.
Hydraulic Transcrestal Maxillary Sinus Floor Elevation
Procedure/SurgeryHydraulic transcrestal maxillary sinus floor elevation with simultaneous implantation in the maxillary molar region.
Treatment groups
Trial outcomes
Primary outcomes
Bone loss
The incidence of bone length, width and height gained in maxillary sinus are evaluated through CBCT imaging for preoperative, the day of surgery, and six months after surgery.
Locations
Sponsors and contacts
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This trial is not recruiting at the moment. You can still explore other options: