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Osteochondritis Dissecans of the Knee (KYSOCD)

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified October 2011 by Pekko Penttila, Kuopio University Hospital.
Recruitment status was:  Enrolling by invitation
Sponsor:
ClinicalTrials.gov Identifier:
NCT01455987
First Posted: October 20, 2011
Last Update Posted: October 20, 2011
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Pekko Penttila, Kuopio University Hospital
  Purpose
Osteochondritis dissecans is a relatively common...

Condition
Osteochondritis Dissecans Juvenile Osteochondritis Dissecans

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Retrospective
Official Title: Outcome of the Knee Osteochonditis Dissecans Patiets in Kuopio University Hospital (1990-2009): A Retropective Analysis

Resource links provided by NLM:


Further study details as provided by Pekko Penttila, Kuopio University Hospital:

Primary Outcome Measures:
  • 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


Secondary Outcome Measures:
  • 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). ]
    Lysholm Knee Score and KOOS are validated subjective questionares assessing outcome after knee surgery/injury.


Estimated Enrollment: 265
Study Start Date: June 2010
Estimated Study Completion Date: December 2013
Estimated Primary Completion Date: December 2012 (Final data collection date for primary outcome measure)
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   Child, Adult, Senior
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
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.
Criteria

Inclusion Criteria:

  • Osteochondritis dissecans diagnosis code (ICD-8 to -10) in the medical records of KUH
  • Knee OCD verified from the medical records

Exclusion Criteria:

-Any other medical condition

  Contacts and Locations
No Contacts or Locations Provided
  More Information

Responsible Party: Pekko Penttila, M.D. Postgraduate student. Resident in Pediatric Surgery, Kuopio University Hospital
ClinicalTrials.gov Identifier: NCT01455987     History of Changes
Other Study ID Numbers: KUH5203050
First Submitted: January 4, 2011
First Posted: October 20, 2011
Last Update Posted: October 20, 2011
Last Verified: October 2011

Keywords provided by Pekko Penttila, Kuopio University Hospital:
Osteochondritis dissecans
Juvenile osteochondritis dissecans
Knee
Osteochondral
Outcome

Additional relevant MeSH terms:
Osteochondritis
Osteochondritis Dissecans
Osteochondrosis
Bone Diseases
Musculoskeletal Diseases
Cartilage Diseases
Connective Tissue Diseases