Evaluation of radiographic and clinical outcomes following Absolut femoral prosthesis and Global acetabular cup total hip replacement surgery

Clinical and Radiological Outcome using the Absolut femoral prosthesis and the Global cup system following total hip arthroplasty in patients with Degenerative Joint Disease

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

ANZCTR

Registry ID

ACTRN12614000318684

Acronym

AGC-COP13S

Enrollment

Registered

2014-03-25

Start date

2014-05-20

Completion date

Unknown

Last updated

2020-01-13

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

Conditions

None listed

Brief summary

Fixation of the femoral stem and acetabular shell in their respective bones can be with cement, specialised coatings or a combination of the two (i.e. stem in cement, acetabulum with porous coating), known as hybrid fixation. The cemented Absolut hip stem with the non-cemented Global acetabular cup will be evaluated following primary total hip replacement surgery.

Interventions

Prospective study evaluating post-operative radiology and clinical outcomes in patients who undergo primary total hip replacement using the Absolut femoral stem and Global acetabular cup. Patients will be recruited over a 2 year period and followed up to 10 years after surgery. Duration of surgery will be as is standard for total hip arthroplasty.

Study design

Allocation

Non-randomised trial

Intervention model

Single group

Primary purpose

Treatment

Masking

Open (masking not used)

Eligibility

Sex/Gender

All

Age

60 Years to No maximum

Healthy volunteers

Inclusion criteria

The individual is diagnosed with a primary diagnosis of Degenerative Joint Disease.

Exclusion criteria

-The individual has an active infection within the affected hip joint. -The individual has had previous total hip replacement or hip fusion of the affected hip joint. -The individual has a neuromuscular or neurosensory deficit which limits the ability to evaluate safety and effectiveness of the device or has a systemic disease that would affect the subject's welfare or overall outcome of the study.

Outcome results