RecruitingNCT02230826

Observational Study to Evaluate Long-Term Outcome in Hip Arthroplasty

Multicentric Observational PMCF Study to Evaluate Long-term Outcome, Performance and Safety of Implantable Devices in Hip Arthroplasty


Sponsor

Corin

Enrollment

2,500 participants

Start Date

May 1, 2014

Study Type

OBSERVATIONAL

Conditions

Summary

This long-term outcomes study is designed to collect safety and efficacy data on designated, commercially available, hip arthroplasty products.


Eligibility

Min Age: 18 Years

Inclusion Criteria3

  • Man or woman \>18 years
  • Subjects with indication of arthroplasty surgery with Corin hip devices which are under assessment as part of this PMCF study
  • Subjects who agreed for study participation.

Exclusion Criteria4

  • Subjects with existing tumour and/or particularly high surgical risk-
  • Subjects with anaesthetic risk class IV or higher
  • Subjects under guardianship and/or unable to follow procedures or matters related to the study (examples: Illiterate, recent psychotic or mania disorders and / or inability to comply with usual follow-up visits.)
  • Contraindications for arthroplasty with a Corin hip devices as per product IFU

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Locations(13)

CHU de Bordeaux - Groupe Hospitalier Pellegrin

Bordeaux, France

clinique Oxford Cannes

Cannes, France

CH Dunkerque

Dunkirk, France

Polyclinique Henin Beaumont

Hénin-Beaumont, France

CHU de Nice

Nice, France

Centre Hospitalier Régionnal d'Orléans - Site La Source

Orléans, France

Clinique Arago

Paris, France

Hôpital de la Croix Saint-Simon

Paris, France

Hopital privé Saint-Martin

Pessac, France

Hôpital Provo

Roubaix, France

Polyclinique St Georges de Didonne

Saint-Georges-de-Didonne, France

Médipôle Garonne

Toulouse, France

Hôpital Jean Bernard

Valenciennes, France

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NCT02230826


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