Total Knee ReplacementNCT01522781
10 Year Outcome of Total Knee Replacement (TKR) Using Sigma Prosthesis
An observational study of Total Knee Replacement, run by NHS Fife at 1 site in United Kingdom.
Trial summary
The purpose of this study is to obtain a prospective database which will allow analysis of total knee outcomes. Read more about this study
- Who is it for?
- Any age
- Conditions the study is for
- Total Knee Replacement
- How many people
- 234 participants
- Where
- 1 siteUnited Kingdom
- Study dates
- Oct 1998to Oct 2008
- 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 Any age
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Study population: All patients undergoing total knee replacement in Fife
Who may be able to join
- All patients undergoing total knee replacement in Fife
Who cannot join
None listed.
Trial locations and contacts
1 site in 1 country.
About this study
The purpose of this study is to obtain a prospective database which will allow analysis of total knee outcomes.
Read the detailed description
A prospective database was set up in October 1998. Patient details are collected pre-operatively, intra-operatively and immediately post operatively. Patients are then followed up in a dedicated knee clinic at 6 months, 18 months, 3 years and 5 years. Data such as SF12 and the American knee society score has been done at each visit.
- Conditions
- Total Knee Replacement
What is being measured
The primary outcome is the main question the study is designed to answer.
Clinical outcome of the Sigma knee at 10 years
Patient satisfaction scores SF 12 and Oxford American Knee society score
Measured: 10 years
Secondary outcomes (1)
Radiographic outcomes at 10 years
looking for failure by identitying lucent lines and osteolysis
Measured: 10 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted1 Feb 2012 (estimated)
- Study startOct 1998
- Primary completionOct 2008
- Study completionOct 2008
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Total Knee ReplacementStudies 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
- Cohort
- Time perspective
- Prospective
- Enrolment
- 234 participants (actual)
Sponsor and investigators
- Lead sponsor
- NHS Fife
- Sponsor type
- Other government
- Collaborators
- DePuy International
- Responsible party
- Principal investigator, Ivan Brenkel, NHS Fife
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01522781
- Sponsor's protocol ID
- IIS2010001
- Status last verified
- Jan 2012
- First submitted
- 24 Jan 2012
- Last updated
- 1 Feb 2012
- Results posted
- No
- Data monitoring committee
- No
Study at a glance
From the registry record, last updated by the sponsor on 1 Feb 2012. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- 10 Year Outcome of Total Knee Replacement (TKR) Using Sigma Prosthesis
- ClinicalTrials.gov ID
- NCT01522781
- Acronym / sponsor ID
- IIS2010001
- Conditions
- Total Knee Replacement
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 234 participants (actual)
- Lead sponsor
- NHS FifeOther government
- Collaborators
- DePuy International
- Study start
- Oct 1998
- Primary completion
- Oct 2008 (actual)
- Study completion
- Oct 2008 (actual)
- First posted
- 1 Feb 2012 (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 obtain a prospective database which will allow analysis of total knee outcomes.
Detailed description
A prospective database was set up in October 1998. Patient details are collected pre-operatively, intra-operatively and immediately post operatively. Patients are then followed up in a dedicated knee clinic at 6 months, 18 months, 3 years and 5 years. Data such as SF12 and the American knee society score has been done at each visit.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
Who may qualify
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
- Study population
- All patients undergoing total knee replacement in Fife
Key inclusion criteria (1 listed)
- All patients undergoing total knee replacement in Fife
Key exclusion criteria (0 listed)
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
Clinical outcome of the Sigma knee at 10 years
Time frame: 10 years
Patient satisfaction scores SF 12 and Oxford American Knee society score
1 secondary outcome
Radiographic outcomes at 10 years
Time frame: 10 years
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 1 Feb 2012.
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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.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Total Knee Replacement, run by NHS Fife at 1 site in United Kingdom.
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 1 inclusion and 0 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: finished, as of the sponsor's last update on 1 Feb 2012. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United Kingdom. Whether a site is taking part right now should be confirmed with that site. See every site.
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 is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
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.
What does the primary outcome measure?
Clinical outcome of the Sigma knee at 10 years (time frame: 10 years). It is what the study was designed to measure, not a finding.
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 1 Feb 2012.