Kepler University Hospital
Linz, 4020, Austria
NCT Number: NCT02915588
The purpose of the study is to compare two different rehabilitation protocols after arthroscopic rotator cuff surgery.
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Notify Me18 year–70 year
All sexes
Interventional
Not applicable
Linz, 4020, Austria
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: up to 24 weeks
Timepoints: Before surgery; 6, 12, 24 weeks after surgery
Time frame: up to 24 weeks
Timepoints Before surgery; 6, 12, 24 weeks after surgery
Time frame: up to 24 weeks
Timepoints: Before surgery; 6, 12, 24 weeks after surgery; Range of movement is measured by handheld goniometer
Time frame: up to 24 weeks
Timepoints: Before surgery; 6, 12, 24 weeks after surgery; Pain is measured by Visual Analogue Scale (0-100mm)
Time frame: up to 24 weeks
Timepoints: Before surgery; 6, 12, 24 weeks after surgery; Measurement of Strength is evaluated using a BTE Simulator II Dynamometer (Peak torque in N).
Johannes Kepler University of Linz
Other
Early Active Rehabilitation After Arthroscopic Rotator Cuff Repair: A Prospective Randomized Pilot Study
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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.
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