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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01158677
Other study ID # 2010/117
Secondary ID
Status Completed
Phase
First received
Last updated
Start date July 2010
Est. completion date July 2015

Study information

Verified date December 2022
Source University Hospital, Ghent
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Completed
Enrollment 150
Est. completion date July 2015
Est. primary completion date July 2015
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion criteria: - all the meniscectomy patients (male & female, all ages) Exclusion Criteria:None

Study Design


Related Conditions & MeSH terms


Intervention

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

Locations

Country Name City State
Belgium University Hospital Ghent Ghent

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Ghent

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary The clinical outcome (residual lesions) after a meniscectomy KOOS-scale, Vas-scale, Tegner questionnaire, SF-36 questionnaire 12 months post-operative
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