Non-Interventional, Multicenter Bicontact® E PMCF Study

Aesculap

Status: Completed

Conditions: Femoral Head Necrosis; Degenerative Osteoarthritis; Femoral Neck Fractures; Rheumatoid Arthritis

Study type: Observational

Funder types: Industry

Identifiers

NCT03442855

AAG-O-H-1417

Details and patient eligibility

About

Prospective observational (non-interventional) cohort study, multi-centric in 5 study Centers in Japan to collect short term clinical and radiological results of the cementless Bicontact® E stem in a standard patient population used in routine clinical practice

Enrollment: 73 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Indication for Bicontact E prosthesis THA
• Patients ≥ 18 years
• Patient not pregnant
• Written informed consent

Exclusion criteria

• Patients receiving a bipolar implantation