Recruitment

Recruitment Status
Active, not recruiting

Summary

Conditions
  • Correction of Functional Deformity
  • Osteoarthritis
  • Rheumatoid Arthritis
Type
Observational
Design
Observational Model: Case-ControlTime Perspective: Retrospective

Participation Requirements

Age
Younger than 125 years

Description

Study Aim: To collect survivorship and clinical outcomes long-term data confirm-ing safety, performance and clinical benefits of the Exceed ABT ce-mentless cup when used in combination with ceramic and polyeth-ylene articulating liners Objectives: Primary Objectives: Clinical performance - as measur...

Study Aim: To collect survivorship and clinical outcomes long-term data confirm-ing safety, performance and clinical benefits of the Exceed ABT ce-mentless cup when used in combination with ceramic and polyeth-ylene articulating liners Objectives: Primary Objectives: Clinical performance - as measured by clinical score data (HHS, WOMAC and Oxford Hip Score), radiographic as-sessments and survivorship which will be based on removal of the device. Secondary Objectives: Safety will be evaluated by monitoring incidence of adverse events. Length of study: 13 years (3 years enrollment plus 10 years follow-up): Post-operative follow-up visits at: 1, 3, 5, 7 and 10 years

Tracking Information

NCT #
NCT04255394
Collaborators
Not Provided
Investigators
Not Provided