Bone Density by Dual Energy X-ray Absorptiometry (DEXA) Following Total Hip Arthroplasty with the Short Mini Stem

Not Applicable

Completed

• Conditions: Degenerative Joint disease; Musculoskeletal - Osteoarthritis

• Registration Number: ACTRN12609001062213
• Lead Sponsor: Smith and Nephew Surgical (local sponsor)

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2009-12-10
• Study Completion: 2016-04-18
• Last Update Posted: 6 November 2023

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

1. Patient has hip disease that requires a total hip arthroplasty
2. Patient is willing to consent to participate in the study
3. Patient plans to be available for the study duration
4. Patient is in stable health and is free of or treated and stabilized for cardiac, pulmonary, haematological, or other conditions that would pose excessive operative risk.

Exclusion Criteria

1. Patient known to have insufficient bone stock
2. Patient has had major non-arthroscopic surgery to the study hip
3. Patient has physical, emotional or neurological conditions that would compromise the patient's compliance with postoperative rehabilitation and follow-up
4. patient has a known sensitivity to materials in the device

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Assess the Bone ingrowth by DEXA and radiographs following implantation[ pre-operative, 3 months, 6 months, 12 months, 2 years, 5 years]

Secondary Outcome Measures

Name	Time	Method
Patient Quality of Life questionnaires[ pre-operative, 3 months, 12 months, 2 years, 3 years, 5 years];Clinical/Functional Evauation including range of motion using the Harris Hip Score (HHS) and Hip Osteoarthritis Outcome Score (HOOS).[ pre-operative, 3 months, 12 months, 2 years, 3 years, 5 years]