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

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00663468
Enrollment
11
Registered
2008-04-22
Start date
2008-04-01
Completion date
2009-09-16
Last updated
2026-08-31

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

Conditions

Hip Fractures

Keywords

determine changes in patient pain level, determine changes in patient functionality, determine changes in patient life quality

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

Interventions

None listed

Sponsors

Phoenix Kinetics
Lead SponsorINDUSTRY

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
Yes

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

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 1, 2026