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Clinical Trials/ACTRN12613000812796
ACTRN12613000812796
Recruiting
N/A

Dislocation, osteolysis, polyethylene wear, acetabular component migration and other complications 7 to 10 years following randomisation to either a large 36 mm or standard 28 mm diameter metal on highly cross-linked polyethylene articulation in total hip replacement

Prof Donald Howie0 sites300 target enrollmentJuly 24, 2013

Overview

Phase
N/A
Intervention
Not specified
Conditions
Dislocation of total hip replacement
Sponsor
Prof Donald Howie
Enrollment
300
Status
Recruiting
Last Updated
6 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
July 24, 2013
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Prof Donald Howie

Eligibility Criteria

Inclusion Criteria

  • Only patients involved in the RCT, ACTRN12609000678291, will be eligible for this study

Exclusion Criteria

  • Not previously enrolled in the RCT, ACTRN12609000678291

Outcomes

Primary Outcomes

Not specified

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