Observational Study to Evaluate Long-Term Outcome in Hip Arthroplasty
Recruiting · NCT02230826 · Observational (researchers observe without assigning treatment) · Lead sponsor: Corin
View the official record on ClinicalTrials.gov →What this trial is about
This long-term outcomes study is designed to collect safety and efficacy data on designated, commercially available, hip arthroplasty products.
Who can take part
Age range
18 Years and older
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not specified
Study type
Observational (researchers observe without assigning treatment)
Inclusion criteria
- 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 criteria
- 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
Where it is running
13 locations listed.
- 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