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Short Term Outcome After Meniscectomy

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 December 2014 by University Hospital, Ghent.
Recruitment status was:  Recruiting
Sponsor:
Information provided by (Responsible Party):
University Hospital, Ghent
ClinicalTrials.gov Identifier:
NCT01158677
First received: July 7, 2010
Last updated: December 4, 2014
Last verified: December 2014
  Purpose

Short term outcome after meniscectomy: a meniscectomy is a very frequent performed orthopedically procedure. The short term outcome is favourable, but some patients keep having residual lesions after surgery.

This prospective study examens the clinical outcome after meniscectomy using questionnaires (KOOS, VAS, SF-36, Tegner) (before the surgery, 3, 6 & 12 months postoperative.) The investigators will also record the further treatment options for the people at risk.


Condition Intervention
Meniscectomy
Procedure: Meniscectomy

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Short Term Outcome After Meniscectomy

Further study details as provided by University Hospital, Ghent:

Primary Outcome Measures:
  • The clinical outcome (residual lesions) after a meniscectomy [ Time Frame: 12 months post-operative ] [ Designated as safety issue: No ]
    KOOS-scale, Vas-scale, Tegner questionnaire, SF-36 questionnaire


Estimated Enrollment: 150
Study Start Date: July 2010
Estimated Study Completion Date: July 2015
Estimated Primary Completion Date: July 2015 (Final data collection date for primary outcome measure)
Intervention Details:
    Procedure: Meniscectomy
    patients undergoing meniscectomy will be asked to complete the KOOS-scale,Vas-scale, Tegner questionnaire, SF-36 questionnaire pre-operatively and at 3, 6 and 12 months post-operatively
  Eligibility

Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
all the meniscectomy patients (male & female, all ages)
Criteria

Inclusion criteria:

  • all the meniscectomy patients (male & female, all ages)

Exclusion Criteria:None

  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01158677

Locations
Belgium
University Hospital Ghent
Ghent, Belgium
Sponsors and Collaborators
University Hospital, Ghent
Investigators
Principal Investigator: Peter Verdonk, MD University Hospital Ghent, Belgium
  More Information

Additional Information:
Responsible Party: University Hospital, Ghent
ClinicalTrials.gov Identifier: NCT01158677     History of Changes
Other Study ID Numbers: 2010/117 
Study First Received: July 7, 2010
Last Updated: December 4, 2014
Health Authority: Belgium: Ethics Committee

Keywords provided by University Hospital, Ghent:
meniscectomy

ClinicalTrials.gov processed this record on December 02, 2016