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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02180685
Other study ID # Danish EC 1-10-72-194-14
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 2009
Est. completion date January 2019

Study information

Verified date January 2019
Source Aarhus University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this present study is to determine which surgery technic provides the best clinical outcome after medial patellofemoral ligament reconstruction comparing suture anchors and screw fixation in medial femoral condyle.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date January 2019
Est. primary completion date January 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

- patella luxation, more than 2 times

Exclusion Criteria:

- cartilage damage (grad 3)

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Anchor fixation


Locations

Country Name City State
Denmark Division of Sports Trauma, Tage-Hansens Gade 2b Aarhus

Sponsors (1)

Lead Sponsor Collaborator
Aarhus University Hospital

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Evaluation of subjective symptoms with a patient reported outcome score Anterior Knee Pain Scale Baseline, 6 months 12 Months, 24 months
Secondary Patient reported outcome scores Tegner Baseline, 6 months 12 Months, 24 months
Secondary Patient reported outcome scores KOOS (Knee injury and osteoarthritis outcome score) Baseline, 6 months 12 Months, 24 months
Secondary Re-operation rate Baseline, 6 months 12 Months, 24 months