Post Market Clinical Follow-up of Dual-mobility Acetabular Cup EUROSCUP MOBILE
NCT ID: NCT04993638
Last Updated: 2024-08-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ACTIVE_NOT_RECRUITING
147 participants
OBSERVATIONAL
2021-06-01
2034-06-30
Brief Summary
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Hip replacement is intended to provide increased patient mobility and reduce pain by replacing the damages hip joint articulation in patients where there is evidence of sufficient sound bone to seat and support the components.
As part of post market vigilance, EUROS will collect data on EUROSCUP MOBILE performances and safety
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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EUROSCUP MOBILE cementless
107 who received cementless version of EUROSCUP MOBILE
hip arthroplasty
Hip prosthesis surgery
EUROSCUP MOBILE cemented
40 who received cemented version of EUROSCUP MOBILE
hip arthroplasty
Hip prosthesis surgery
Interventions
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hip arthroplasty
Hip prosthesis surgery
Eligibility Criteria
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Inclusion Criteria
* Patient informed of its participation to the study
* Patient aged between 18 and 80 years old (\<80).
Exclusion Criteria
* Patient who refused to participate to the study
* Vulnerable subjects
18 Years
80 Years
ALL
No
Sponsors
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EUROS
INDUSTRY
Responsible Party
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Locations
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Clinique Montagard
Avignon, , France
CHU Gabriel Montpied
Clermont-Ferrand, , France
Hôpital Saint Joseph-Saint Luc
Lyon, , France
Countries
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Other Identifiers
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EC-310-02-01-A
Identifier Type: -
Identifier Source: org_study_id
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