Osteochondritis Dissecans of the Knee (KYSOCD)

October 19, 2011 updated by: Pekko Penttila, Kuopio University Hospital

Outcome of the Knee Osteochonditis Dissecans Patiets in Kuopio University Hospital (1990-2009): A Retropective Analysis

Osteochondritis dissecans is a relatively common...

Study Overview

Status

Unknown

Conditions

Study Type

Observational

Enrollment (Anticipated)

265

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • ADULT
  • OLDER_ADULT
  • CHILD

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

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.

Description

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

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
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
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 Outcome Measures

Outcome Measure
Measure Description
Time Frame
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.
At the time of recruiting, which is an avarage calculated from all participiants enrolled for this study (estimated avarage follow-up 12-16 years).

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Kuopio University Hospital

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

June 1, 2010

Primary Completion (ANTICIPATED)

December 1, 2012

Study Completion (ANTICIPATED)

December 1, 2013

Study Registration Dates

First Submitted

January 4, 2011

First Submitted That Met QC Criteria

October 19, 2011

First Posted (ESTIMATE)

October 20, 2011

Study Record Updates

Last Update Posted (ESTIMATE)

October 20, 2011

Last Update Submitted That Met QC Criteria

October 19, 2011

Last Verified

October 1, 2011

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • KUH5203050

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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