Clinical Trials Directory

Trials / Terminated

TerminatedNCT02435420

A Retro-prospective Study of Total Hip Arthroplasty With EMPERION Modular Primary Stem in Australian Centres (HISTORIC)

A Retro-prospective Study of Total Hip Arthroplasty With EMPERION Modular Primary Stem in Australian Centres

Status
Terminated
Phase
Study type
Observational
Enrollment
25 (actual)
Sponsor
Smith & Nephew, Inc. · Industry
Sex
All
Age
Healthy volunteers
Not accepted

Summary

This is a retro-prospective, single arm, sequential enrolment study to collect relevant clinical and radiological data in at least 156 subjects, at up to 10 sites in Australia, who have been implanted with the EMPERION™ Modular Hip System in primary THA procedures to assess its safety and efficacy over 5 years post-surgery.

Detailed description

The main aim of the study is to demonstrate that there is no significant difference in survivorship at 5 years in the EMPERION™ primary stem compared to other primary stems for total hip arthroplasty. Investigational site personnel will review and screen clinical records for potential subjects to be included in the study. Eligible patients will be contacted and follow-up status and implant revision status will be assessed at this initial contact. The subject will be given the option to participate in a prospective 5-year on-site follow-up visit for which they will provide written informed consent. An HREC waiver of informed consent for study participation will be obtained for subjects who are lost to follow-up, deceased or are unwilling/unable to participate in a prospective on-site 5-year follow-up visit, allowing the inclusion of data from all patients implanted with the study device regardless of follow-up status and therefore eliminate selection bias. Data will be collected retrospectively from the subject pre-surgery, during surgery, at discharge and at 1-year follow-up found in their medical files and prospective data will be collected from the subject's 5-year Follow-up visit and documented on specially designed Case Report Forms (CRFs). Data to be collected include: * Subject demographics * Primary diagnosis for THA * Additional relevant history and physical findings * Post-operative follow-up findings at 1 and 5 years * Radiological Assessment * Revision by time points * Adverse Events

Conditions

Interventions

TypeNameDescription
DEVICEEMPERION Modular Primary StemPrimary total hip arthroplasty using the EMPERION Modular Primary Stem

Timeline

Start date
2015-08-01
Primary completion
2017-11-09
Completion
2017-11-09
First posted
2015-05-06
Last updated
2018-02-05

Locations

8 sites across 1 country: Australia

Source: ClinicalTrials.gov record NCT02435420. Inclusion in this directory is not an endorsement.