Hip FracturesNCT00663468
Treatment of Sub-capital Fractures of Hip Joint by Using TriboFit™ Acetabular Buffer
An observational study of Hip Fractures, run by Phoenix Kinetics.
Trial 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 Read more about this study
- Who is it for?
- Ages 60 years and olderHealthy volunteers can take part
- Conditions the study is for
- Hip Fractures
- How many people
- 11 participants
- Where
- No sites listed yet
- Study dates
- Apr 2008to 16 Sep 2009
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 60 years and older
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Study population: community sample
Who may be able to join
- 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
Who cannot join
- 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
About this study
The purpose of this study is to determine the performance and efficacy during 6 and 12 month post operation.
- determine changes in patient pain level
- determine changes in patient functionality
- determine changes in patient life quality
- Conditions
- Hip Fractures
- Keywords
- determine changes in patient pain level, determine changes in patient functionality, determine changes in patient life quality
- Medical subject headings
- Hip Fractures
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| A | Not described |
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted22 Apr 2008 (estimated)
- Study startApr 2008
- Primary completion16 Sep 2009
- Study completion16 Sep 2009
Why it stopped: Lead surgeon retired.
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Hip FracturesStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Case only
- Time perspective
- Prospective
- Enrolment
- 11 participants (actual)
Sponsor and investigators
- Lead sponsor
- Phoenix Kinetics
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00663468
- Sponsor's protocol ID
- TLV-0021-08
- Status last verified
- Aug 2026
- First submitted
- 17 Apr 2008
- Last updated
- 31 Aug 2026
- Results posted
- No
Study at a glance
From the registry record, last updated by the sponsor on 31 Aug 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Treatment of Sub-capital Fractures of Hip Joint by Using TriboFit™ Acetabular Buffer
- ClinicalTrials.gov ID
- NCT00663468
- Acronym / sponsor ID
- TLV-0021-08
- Conditions
- Hip Fractures
- Keywords
- determine changes in patient pain level, determine changes in patient functionality, determine changes in patient life quality
- Study type
- Observational
- Recruitment status
- TerminatedReason stopped: Lead surgeon retired.
- Enrolment
- 11 participants (actual)
- Lead sponsor
- Phoenix KineticsIndustry (pharma, biotech, devices)
- Study start
- Apr 2008
- Primary completion
- 16 Sep 2009 (actual)
- Study completion
- 16 Sep 2009 (actual)
- First posted
- 22 Apr 2008 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The purpose of this study is to determine the performance and efficacy during 6 and 12 month post operation.
- determine changes in patient pain level
- determine changes in patient functionality
- determine changes in patient life quality
Study design
- Observational model
- Case only
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| A | – | – |
Who may qualify
- Ages
- 60 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
- Study population
- community sample
Key inclusion criteria (8 listed)
- 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
Key exclusion criteria (8 listed)
- 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
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Not reported in the source record.
Results and safety
The study was stopped early (reason given: Lead surgeon retired.). Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 31 Aug 2026.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
Questions about this trial
What is this clinical trial studying?
An observational study of Hip Fractures, run by Phoenix Kinetics.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 8 inclusion and 8 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: stopped early, as of the sponsor's last update on 31 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study was stopped early (reason given: Lead surgeon retired.). Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 31 Aug 2026.