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Knee Arthroscopy Cohort Southern Denmark (KACS)

Knee Arthroscopy Cohort Southern Denmark (KACS)

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01871272
Acronym
KACS
Enrollment
491
Registered
2013-06-06
Start date
2013-02-28
Completion date
2015-06-30
Last updated
2015-06-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Knee Osteoarthritis, Meniscus Injury

Brief summary

PURPOSE: To investigate the natural time course of patient-reported outcomes after meniscus surgery and identify factors associated with good and bad outcome after surgery.

Interventions

Surgery to the meniscus - resection or repair.

Sponsors

Odense University Hospital
CollaboratorOTHER
Lillebaelt Hospital, Kolding and Vejle, Denmark
CollaboratorUNKNOWN
University of Southern Denmark
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Assigned for arthroscopy on suspicion of a medial and/or lateral meniscus tear. * Age \>18 years at time of recruitment * Having an email address * Able to read and understand Danish

Exclusion criteria

* Patients who will or have previously undergone surgical reconstruction of the anterior or posterior cruciate ligament (ACL or PCL) in either knee * Fracture to the lower extremities (i.e. hip, leg or foot) in either leg within the last 6 months prior to recruitment * Not mentally able to reply to the questionnaire

Design outcomes

Primary

MeasureTime frameDescription
Knee Injury and Osteoarthritis Outcome Score (KOOS)PRE surgery (assessed 1-14 days prior to surgery) and at 12 weeks and 52 weeks follow-upKnee specific questionnaire. All domains on the KOOS. Primary end point is change from PRE surgery (assessed 1-14 days prior to surgery) to 52 weeks follow-up.

Secondary

MeasureTime frameDescription
Medical Outcomes Study 36-Item Short Form Health Survey (SF-36)PRE surgery (assessed 1-14 days prior to surgery) and at 12 weeks and 52 weeks follow-up.Generic health survey questionnaire.
Patient Acceptable Symptom State (PASS)At 12 weeks and 52 weeks follow-up.Dichotomous outcome (y/n) to the question: Considering your knee function, do you feel that your current state is satisfactory? With knee function you should take into account all activities you have during your daily life, sport and recreational activities, your level of pain and other symptoms, and also your knee related quality of life.
Treatment failure (TF)At 12 weeks and 52 weeks follow-up.Patients replying no to the PASS question will also be asked to answer (y/n) the following question: Would you consider your current state as being so unsatisfactory that you think the treatment has failed?. Patients replying, yes to the second question will be defined as experiencing treatment failure (TF).

Other

MeasureTime frameDescription
Global perceived effect (GPE)At 12 weeks and 52 weeks follow-up.Questions regarding global perceived effect (GPE) to explore minimal clinical important change in patient-reported outcomes.

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 10, 2026