Division of Sports Trauma, Tage-Hansens Gade 2b
Aarhus, 8000, Denmark
NCT Number: NCT02680821
Patients with combined Anterolateral ligament (ALL) reconstruction- Anterior cruciate ligament (ACL) revision will have a better rotational knee stability and therefore better patient reported outcome measure (PROM) scores compared to patients, who have ACL revision surgery without ALL reconstruction.
Looking for future studies?
Notify Me18 year–50 year
All sexes
Interventional
Not applicable
Aarhus, 8000, Denmark
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: 12 months
questionaire
Time frame: 12 Months
questionaire
Time frame: 12 Months
Objective Knee stability
Time frame: 12 Months
questionaire
Aarhus University Hospital
Other
Effect of Reconstruction of the Anterolateral Ligament (ALL) in Combination With Revision Anterior Cruciate Ligament (ACL) Surgery. A Clinical Randomized Trial
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT00478894
Anterior Cruciate Ligament Injuries, Arthritis
St Louis, Missouri, United States
View Trial DetailsNCT02374710
Anterior Cruciate Ligament Injuries, Complete Tear, Knee, Anterior Cruciate Ligament
Charlottesville, Virginia, United States
View Trial DetailsNCT01069588
Anterior Cruciate Ligament Injuries, Knee Injuries
Nashville, Tennessee, United States
View Trial DetailsNCT04431063
Anterior Cruciate Ligament Injuries, Knee Injuries
Jakarta, DKI Jakarta, Indonesia
View Trial Details