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Short-Term Clinical Outcome of Total Hip Arthroplasty Using Larger Diameter of 4th Generation Ceramic Bearing

Short-Term Clinical Outcome Including Dislocation Rate and Ceramic Fracture of Total Hip Arthroplasty Using Larger Diameter of 4th Generation Ceramic Bearing

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01103882
Enrollment
277
Registered
2010-04-15
Start date
2010-05-31
Completion date
2017-12-31
Last updated
2018-06-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Arthropathy of Hip

Brief summary

The primary objectives of this clinical study include: * Assess the rate of dislocation and fracture of THA using the new (the 4th generation) ceramic implants. * Evaluate the survival rate of THA using the new alumina-zirconia (the 4th generation) composite ceramic bearing. * Investigate the performance of the 4th generation ceramic implants mostly in patients younger than 50 years. * Compare the preoperative and postoperative scores of Harris Hip Score, UCLA Activity Score and WOMAC.

Detailed description

This study will evaluate incidence of dislocation and short-term clinical outcome on patients who undergo large diameter 4th generation ceramic bearing total hip Arthroplasty (THA) in comparison to historical data on 3rd generation CoC THA (28mm) patients. Specifically the study intends to address the following research topics: 1. The incidence of dislocation after THA with use of the 4th generation Ceramic Bearing in comparison to 3rd generation Ceramic Bearing. 2. The incidence of ceramic fracture after THA with use of the 4th generation Ceramic Bearing in comparison to 3rd generation Ceramic Bearing 3. The survival rate, wear rate, and incidence of osteolysis of THA with use of the 4th generation Ceramic Bearing 4. Range of motion improvement from preoperative to postoperative to support Korean sitting style after THA with use of the 4th generation Ceramic Bearing. 5. Clinical outcomes, activity level and QoL of patients with use of the 4th generation Ceramic Bearing. 6. The performance of THA with use of the new ceramic bearing mostly in patients younger than 50 years.

Interventions

None listed

Sponsors

Zimmer Biomet
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients suitable for primary Total Hip Replacement * Patients with degenerative joint disease (inflammatory or non-inflammatory) or any of the composite diagnoses of: 1. Osteoarthritis 2. Avascular necrosis 3. Legg Perthes 4. Rheumatoid Arthritis 5. Diastrophic variant 6. Fracture of the pelvis 7. Fused hip 8. Slipped capital epiphysis 9. Subcapital fractures 10. Traumatic arthritis * Patients aged over 20 * Patients must be able to understand instructions and be willing to return for follow-up

Exclusion criteria

* Absolute contraindications include: infection, sepsis, and osteomyelitis * Relative contraindications include: 1. uncooperative patient or patient with neurologic disorders who are incapable of following directions, 2. osteoporosis, 3. metabolic disorders which may impair bone formation, 4. osteomalacia, 5. distant foci of infections which may spread to the implant site, 6. rapid joint destruction, marked bone loss or bone resorption apparent on roentgenogram, and 7. vascular insufficiency, muscular atrophy, or neuromuscular disease. 8. pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Dislocation12 month postopNumber of dislocations

Secondary

MeasureTime frameDescription
Clinical Outcomes12 months, 18 months and 30 monthsHarris Hip Score, UCLA and WOMAC

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026