Prevision® PMCF Study

Aesculap

Status: Completed

Conditions: Survival, Prosthesis

Treatments: Device: Prevision®

Study type: Observational

Funder types: Industry

Identifiers

NCT03510065

AAG-O-H-1508

Details and patient eligibility

About

Monocentric, non-interventional Post-Market Clinical Follow-Up (PMCF) Study on past implantations of the Prevision® prosthesis; the survival rate of the Prevision® prosthesis shall be evaluated and compared to literature results on comparable Revision stems.

Enrollment: 150 patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion:

• Patient received a Prevision® Hip Stem (curved or straight) between 2002 an 2012
• Patient gave his written consent for study participation

Exclusion:

• none