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Safety and Performance Assessment of the SYMBOL Range of Medical Devices in Patients Underlying Total Hip Arthroplasty

Recruitingn/aAges 18 Years - anyAllDedienne Sante S.A.S.
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In plain words

What the trial is, and whether it could suit you

The purpose of this post-market clinical follow up study is to assess the safety and effectiveness of the SYMBOL range of medical devices. The study will evaluate the outcome of Total Hip Arthroplasty using medical devices from SYMBOL range over a period of 10 years.

Sign in to get the eligibility rules as simple questions to take to your doctor.

📋 Eligibility rules (as published)
Inclusion Criteria: * Patient age \> 18 years at implantation. * Patient who will undergo, during the study's period of inclusion, a total hip arthroplasty (primary or revision) with at least one SYMBOL medical device (DEDIENNE Santé). * Patient informed of his/her participation and willing to participate in the study. * Patient able to read, write and understand French. Exclusion Criteria: * Patient deprived of freedom, under guardianship/curatorship or placed under judicial protection * Patient unable to follow study procedures. * Patient who has already been included in the study for a total hip arthroplasty (primary or revision) with at least one SYMBOL medical device.
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What it tests

  • Total hip arthroplasty (primary or revision)
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Where

9 sites
Hôpital Privé de la Châtaigneraie
Beaumont, France
CH de Marmande - CHIC
Marmande, France
Hôpital Privé du Grand Narbonne
Montredon-des-Corbières, France
Polyclinique Grand Sud
Nîmes, France
Clinique Mutualiste Catalane
Perpignan, France
CH de Péronne
Péronne, France
Clinique Mutualiste
Saint-Etienne, France
Hôpital d'Instruction des Armées Saint-Anne
Toulon, France

…and 1 more on ClinicalTrials.gov.

🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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