Success and Safety of the Implant Placement Using Navigated Surgery

ConditionEdentulism
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorRoberto Villa

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

No treatment groups listed

Locations

This trial has no locations

Sponsors and collaborators

Roberto Villa

Lead sponsor

Clinica Odontoiatrica Villa

Sponsor institution

Nobel Biocare Services AG

Collaborator