A prospective, observational case series to assess the clinical utility of improved methods of functional hip navigation for total hip replacement

Not Applicable

Completed

• Conditions: Osteoarthritis; Rheumatoid arthritis; Avascular necrosis; Musculoskeletal - Osteoarthritis; Musculoskeletal - Other muscular and skeletal disorders

• Registration Number: ACTRN12609001030268
• Lead Sponsor: Stryker Australia

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2009-11-27
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 150

Inclusion Criteria

1. Patient is a candidate for primary total hip replacement using computer navigation.
2. Patient has a primary diagnosis of osteoarthritis, rheumatoid arthritis or avascular necrosis.
3. Patient is a male or non-pregnant female patient age 18 to 90.
4. Patient has signed a Human Research Ethics Committee (HREC)-approved, study specific Information Patient Consent Form.

Exclusion Criteria

1. Patient has abnormal pelvic anatomy (previous fracture, osteotomy or development dysplasia).
2. Patient is morbidly obese (Body Mass Index, BMI >= 40).
3. Patient has an existing condition where increasing surgical time may be detrimental to the patient.
4. Patient has a cognitive impairment, an intellectual disability or a mental illness.

Study & Design

• Study Type: Observational
• Study Design: Not specified