About this trial
This study aims to collect real-world clinical data to gather information on the performance and safety of the Neocement® Inject P when used according to its intended purpose and current clinical applications. The results of the clinical study will serve as clinical evidence for the device's clinical evaluation.
Eligibility criteria
Qualifiers
Adult males or females (age > 18 years old);
Patients who are able to sign an informed consent form (for data collection);
Patients undergoing reconstructive dental surgery and indicated for the use of Neocement® Inject P;
Disqualifiers
Patients who are unable to understand consent and the objectives of the study;
Signs of local or systemic acute/ active or chronic infections;
Metabolic affections;
Severe degenerative diseases, conditions in which general bone grafting is not advisable;
Trial design
Treatments tested in this trial
- Not listed
Trial groups
Sponsors and collaborators
Bioceramed
Lead sponsor
Egas Moniz - Cooperativa de Ensino Superior, CRL
Collaborator