Treatment of Sub-capital Fractures of Hip Joint by Using TriboFit™ Acetabular Buffer

Terminated

• Conditions: Hip Fractures

• Registration Number: NCT00663468
• Lead Sponsor: Active Implants

Brief Summary

The purpose of this study is to determine the performance and efficacy during 6 and 12 month post operation.

1. determine changes in patient pain level

2. determine changes in patient functionality

3. determine changes in patient life quality

Detailed Description

Not available

Study Timeline

• Study Start: 2008-04
• Study First Submitted: 2008-04-17
• Study First Submitted QC: 2008-04-21
• Study First Posted: 2008-04-22
• Primary Completion: 2009-09-16
• Study Completion: 2009-09-16
• Status Verified: 2020-02
• Last Update Submitted: 2020-02-11
• Last Update Posted: 2020-02-12

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 11

Inclusion Criteria

• Female or male that is not younger than 60 years old.
• Patient suffers from hip fracture that will need hip arthroplasty.
• Patient that weight less than 150Kg
• Patient femur head diameter between 40mm - 50mm
• Mentally normal
• Patient that could walk before suffering from hip fracture
• Patient that willing to cooperate with the doctor
• Patient that signed on the acceptance form

Exclusion Criteria

• Patient that does not willing to cooperate with the doctor
• Patient that is legally rejected
• Patient that suffer from cancer
• Patient that had passed amputation in is limbs
• Patient that is paralysis
• Patient that passed CVA or TIA
• Patient that still recovering from hard wounds or surgery
• Patient that suffer from infection in the hip joint

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified