About this trial
Subjects with severely atrophic mandibles were treated with implants and implant-based restorations. Subjects will be required to consent to study participation and data processing according to General Data Protection Regulation (GDPR). Implant positions were planned digitally in a dental software DTX Studio, and implants placed with navigated surgery (Nobel Biocare X-Guide). Implants eligible for this study must be placed 2 mm or less from the alveolar nerve. Implants placed are NobelParallel TiUnite and NobelActive TiUnite. All subjects were followed up for 1 year after surgery to monitor success and adverse events related to the alveolar nerve. Data analysis will include demographics, medical history, Cone-beam Computed Tomography (CBCT) scans/peri-apical x-ray data, soft tissue parameters, and adverse events.
Eligibility criteria
Qualifiers
Implants placed in 2 mm distance or less of the alveolar nerve
Subject was at least 18 years old at the time of surgery
Subject signed consent form
Subject signed GDPR form
Disqualifiers
1-year follow-up data on treatment success not available
Trial design
Treatments tested in this trial
- implant placement using navigated surgery near alveolar nerve
Treatment groups
Locations
Sponsors and collaborators
Roberto Villa
Lead sponsor
Clinica Odontoiatrica Villa
Sponsor institution
Nobel Biocare Services AG
Collaborator