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Study identifier: NCT06354543 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Arthroplasty Cements Outcomes - A Post-market Follow-up

Condition: Arthroplasty  ·  Sponsor: Teknimed

PhaseN/A
Planned participants1050
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

A Post-Market Clinical Follow-Up (PMCF) Study to collect clinical data on safety and performance of all Teknimed Arthroplasty range of products: CEMFIX® and GENTAFIX® bone cements families and CEMSTOP® cement restrictor, and all their private labels. Teknimed bone cements and cement restrictor are legacy products, some marketed for more than 20 years. Their performance and safety have already been demonstrated by Post-Market Surveillance and previous clinical studies. The current Post-Market Clinical Follow-Up study aims to confirm these claims by collecting data in a "real-life" setting. The study is a retrospective and prospective global, single arm, non-controlled, multicentric, ambispective observational study. Patients will be followed as per local standard medical care of the site.

This description comes directly from the study's public registry record.

Talk to the study team

Solange VAN DE MOORTELE, PhD  ·  +33 5 34 25 26 79  ·  s.vandemoortele@teknimed.com

Always discuss trial participation with your own doctor first.

Locations (10)

CH de BriveBrive-la-Gaillarde, Aquitaine, FranceRecruiting
Clinique du VivaraisAubenas, Auvergne-Rhône-Alpes, FranceRecruiting
Clinique du Val d'OuestÉcully, Auvergne-Rhône-Alpes, FranceRecruiting
Cabinet de consultationÉvreux, Eure, FranceRecruiting
Clinique de l'AtlantiquePuilboreau, New Aquitaine, FranceRecruiting
Clinique du Dr Henri GuillardCoutances, Normandy, FranceRecruiting
MIROUSEBoujan-sur-Libron, Occitanie, FranceRecruiting
Hôpital Européen MarseilleMarseille, Provence-Alpes-Côte d'Azur Region, FranceRecruiting
Instituto Ortopedico RizzoliBologna, Emilia-Romagna, ItalyRecruiting
Ospedale Santissima AnnunziataCento, Emilia-Romagna, ItalyRecruiting

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Source record: clinicaltrials.gov/study/NCT06354543