Investigation to Determine Safety of Taperloc Stems With BioGuard Coating When Used in Cementless Total Hip Arthroplasty

NAActive, not recruitingINTERVENTIONAL

Enrollment

Participants

Timeline

Start Date

October 31, 2013

Primary Completion Date

November 30, 2015

Study Completion Date

May 31, 2025

Conditions

Osteoarthritis of Hip

Interventions

DEVICE

Bioguard Group

Patients randomised to receive the study investigative device will receive a Bioguard implant

DEVICE

Control Group

Patients randomised to receive the control device will receive a Exceed Taperlock implant

Trial Locations (1)

RJAH, Oswestry