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Evaluation of the Safety and Performance of the TriOSS®: A Prospective Observational Study in Dental Area

NCT06813885 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 80

Last updated 2026-02-03

No results posted yet for this study

Summary

This study aims to collect real-world clinical data to gather information on the performance and safety of the TriOSS® 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, targeting submission to the new Medical Device Regulation (EU) 2017/745.

Conditions

  • Bone Augmentation

Sponsors & Collaborators

  • Egas Moniz - Cooperativa de Ensino Superior, CRL

    collaborator OTHER

  • Bioceramed

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-03-05
Primary Completion
2027-02-28
Completion
2027-02-28

Countries

  • Portugal

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06813885 on ClinicalTrials.gov