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MRI scanning for soft tissue pathology after total hip arthroplasty. A feasibility study study of a selected cohort

MRI scanning for soft tissue pathology after total hip arthroplasty. A feasibility study study of a selected cohort - MRI scanning for soft tissue pathology after total hip arthroplasty

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON38432
Enrollment
50
Registered
2013-08-13
Start date
2013-04-19
Completion date
Unknown
Last updated
2024-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cyste metalosis

Interventions

None listed

Sponsors

Biomet inc
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Unilateral, non-revised ceramic-on-polyethylene total hip arthroplasty

Exclusion criteria

Exclusion criteria: Revision surgery. Bi-lateral hip prosthesis. Proven instability. Contra-indication for MRI scanning. Infection

Design outcomes

Primary

MeasureTime frame
Main study parameter is the occurrence and details (frequency, form, size, location) of cyst formation or other MRI abnormalities in patients with Ceramic-on-Polyethylene bearings who theoretically are prone to cyst formation.

Secondary

MeasureTime frame
Kobalt and Chromium serum concentration in perspective to the cyst. Relation of clinical outcome and cysts.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)