Clinical Trial

Evaluation of the Safety and Performance of the TriOSS®: A Retrospective Observational Study in Orthopaedic Area

Study acronym: TriOSSOrto01
Terminated
View on ClinicalTrials.gov →
Why the trial stopped
The study was terminated prematurely due to the inability to collect retrospective clinical data within the required contractual and regulatory deadlines. Although ethical approval was obtained, data collection was not performed.
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.
Protocol Amendment History 2 amendments
This ClinicalTrials.gov record has been amended 2 times since 2025-07-18; most recent amendment 2026-02-02.
Status change: Active, Not Recruiting → Terminated 2026-02-02
Status change: Not Yet Recruiting → Active, Not Recruiting 2025-10-01
Trial Details
NCT Number NCT07087509
Lead Sponsor Bioceramed
Collaborators: Hospital dos Lusíadas
Conditions Bone Defect, Orthopedic
Enrollment 23 participants
Start Date 2025-09-30
Primary Completion 2026-01-05 (estimated)
Study Completion 2026-01-05 (estimated)
Updated on ClinicalTrials.gov 2026-02-04