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ACTIVE NOT RECRUITING
NCT02149667

Post Market Clinical Follow-up Study Protocol for DYNASTY® BioFoam® Acetabular Components

Sponsor: MicroPort Orthopedics Inc.

View on ClinicalTrials.gov

Summary

Sponsor is conducting this post market clinical follow-up (PMCF) study to evaluate the safety and efficacy of its total hip arthroplasty (THA) components marketed in the European Union (EU) . These types of studies are required by regulatory authorities for all THA devices that do not have medium to long-term clinical evidence available at the time of gaining approval to market in the EU. This study has been designed in accordance with MEDDEV 2.12/2 rev 2.

Key Details

Gender

All

Age Range

21 Years - Any

Study Type

OBSERVATIONAL

Enrollment

48

Start Date

2014-12

Completion Date

2028-12

Last Updated

2023-06-07

Healthy Volunteers

No

Conditions

Interventions

DEVICE

total hip arthroplasty implant

Locations (1)

Ottawa Hospital

Ottawa, Ontario, Canada