Follow-Up of the Prevision® Hip Stem (PRESPECT)

Aesculap

Status: Completed

Conditions: Periprosthetic Fracture Around Prosthetic Joint Implant; Aseptic Loosening of Prosthetic Joint

Study type: Observational

Funder types: Industry

Identifiers

NCT04833634

AAG-O-H-2008

Details and patient eligibility

About

The main objective of this study is to represent the treatment reality at the study site and to draw conclusions from cases of failure or suboptimal outcome. Potential risk factors for revision surgery, suboptimal outcome or radiologic sign of loosening, bone non-union or stem subsidence will be evaluated. Next to the functional outcome, stem subsidence will be used as an important indicator for a stable fixation of the revision stem.

Enrollment: 46 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• All patients implanted with a Prevision® hip stem at the study site between 2014 and 2019
• Written informed patient consent

Exclusion criteria

• Patients < 18 years at surgery