Evaluation of the Safety and Performance of the Neocement® Inject P: A Prospective Observational Study in Dental Area

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorBioceramed

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

No trial groups listed

Sponsors and collaborators

Bioceramed

Lead sponsor

Egas Moniz - Cooperativa de Ensino Superior, CRL

Collaborator