Osteochondritis DissecansKYSOCDNCT01455987
Osteochondritis Dissecans of the Knee
An observational study of Osteochondritis Dissecans and Juvenile Osteochondritis Dissecans, run by Kuopio University Hospital.
Trial summary
Osteochondritis dissecans is a relatively common... Read more about this study
- Who is it for?
- Any age
- Conditions the study is for
- Osteochondritis Dissecans, Juvenile Osteochondritis Dissecans
- How many people
- 265 participants
- Where
- No sites listed yet
- Study dates
- Jun 2010to Dec 2013
- 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: Patients who have been treated in Kuopio University Hospital (KUH) district for osteochondritis dissecans of the knee between 1.1.1990 and 31.12.2009.
Who may be able to join
- Osteochondritis dissecans diagnosis code (ICD-8 to -10) in the medical records of KUH
- Knee OCD verified from the medical records
Who cannot join
- -Any other medical condition
About this study
Official title: Outcome of the Knee Osteochonditis Dissecans Patiets in Kuopio University Hospital (1990-2009): A Retropective Analysis
Osteochondritis dissecans is a relatively common...
- Keywords
- Osteochondritis dissecans, Juvenile osteochondritis dissecans, Knee, Osteochondral, Outcome
- Medical subject headings
- Osteochondritis Dissecans
What is being measured
The primary outcome is the main question the study is designed to answer.
Knee pain measured by NRS (numeric rating scale, 0-10)
0=no pain 10=maximal pain
Measured: At the time of recruiting, which is an avarage calculated from all participiants enrolled for this study (estimated avarage follow-up 12-16 years).
Secondary outcomes (1)
Lysholm Knee Score and Knee Injury and Osteoarthritis Outcome Score (KOOS)
Lysholm Knee Score and KOOS are validated subjective questionares assessing outcome after knee surgery/injury.
Measured: At the time of recruiting, which is an avarage calculated from all participiants enrolled for this study (estimated avarage follow-up 12-16 years).
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted20 Oct 2011 (estimated)
- Study startJun 2010
- Primary completionDec 2012 (estimated)
- Study completionDec 2013 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Osteochondritis DissecansStudies 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
- Retrospective
- Enrolment
- 265 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Kuopio University Hospital
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Pekko Penttila, Kuopio University Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01455987
- Sponsor's protocol ID
- KUH5203050
- Acronym
- KYSOCD
- Status last verified
- Oct 2011
- First submitted
- 4 Jan 2011
- Last updated
- 20 Oct 2011
- Results posted
- No
Study at a glance
From the registry record, last updated by the sponsor on 20 Oct 2011. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Outcome of the Knee Osteochonditis Dissecans Patiets in Kuopio University Hospital (1990-2009): A Retropective Analysis
- ClinicalTrials.gov ID
- NCT01455987
- Acronym / sponsor ID
- KYSOCD / KUH5203050
- Keywords
- Osteochondritis dissecans, Juvenile osteochondritis dissecans, Knee, Osteochondral, Outcome
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 265 participants (estimated)
- Lead sponsor
- Kuopio University HospitalUniversity, hospital or other
- Study start
- Jun 2010
- Primary completion
- Dec 2012 (estimated)
- Study completion
- Dec 2013 (estimated)
- First posted
- 20 Oct 2011 (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.
Osteochondritis dissecans is a relatively common...
Study design
- Observational model
- Cohort
- Time perspective
- Retrospective
Who may qualify
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
- Study population
- Patients who have been treated in Kuopio University Hospital (KUH) district for osteochondritis dissecans of the knee between 1.1.1990 and 31.12.2009.
Key inclusion criteria (2 listed)
- Osteochondritis dissecans diagnosis code (ICD-8 to -10) in the medical records of KUH
- Knee OCD verified from the medical records
Key exclusion criteria (1 listed)
- -Any other medical condition
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
Knee pain measured by NRS (numeric rating scale, 0-10)
Time frame: At the time of recruiting, which is an avarage calculated from all participiants enrolled for this study (estimated avarage follow-up 12-16 years).
0=no pain 10=maximal pain
1 secondary outcome
Lysholm Knee Score and Knee Injury and Osteoarthritis Outcome Score (KOOS)
Time frame: At the time of recruiting, which is an avarage calculated from all participiants enrolled for this study (estimated avarage follow-up 12-16 years).
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 20 Oct 2011.
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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 Osteochondritis Dissecans and Juvenile Osteochondritis Dissecans, run by Kuopio University Hospital.
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 2 inclusion and 1 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: status not confirmed, as of the sponsor's last update on 20 Oct 2011. 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?
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.
What does the primary outcome measure?
Knee pain measured by NRS (numeric rating scale, 0-10) (time frame: At the time of recruiting, which is an avarage calculated from all participiants enrolled for this study (estimated avarage follow-up 12-16 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 20 Oct 2011.