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Clinical Trial Summary

It was conducted a prospective study with a series of 63 patients treated with O.R.I.F. (Open Reduction and Internal Fixation) (group A) and with RSA (Reverse Shoulder Arthroplasty) (group B) for three and four-part proximal humeral fractures according to Neer classification system. One independent observer performed clinical and a psychological evaluation at one(T0), six(T1) and twelve months(T2) postoperatively. The Constant's score and The Disabilities of the Arm, Shoulder and Hand (DASH score) were used for clinical evaluation, while General Anxiety Disorder-7 (GAD-7) and Caregiver Strain Scale (CSS) were used for psychological evaluation.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04821180
Study type Observational
Source Azienda Ospedaliero-Universitaria Consorziale Policlinico di Bari
Contact
Status Completed
Phase
Start date January 2016
Completion date March 2021

See also
  Status Clinical Trial Phase
Completed NCT03383991 - Reverse Total Shoulder Arthroplasty Versus Hemiarthroplasty for Displaced 3- and 4-part Proximal Humeral Fractures N/A
Not yet recruiting NCT03358784 - Comparison of Hemi-shoulder Arthroplasty and PHILOS in Treating Three or Four-part Fractures of Proximal Humerus N/A
Completed NCT03023956 - Outcome of Proximal Humerus Fractures :Anatomic Neck Fractures vs Surgical Neck Fractures N/A
Recruiting NCT04113044 - Go Fit Fast, Recovery Trajectory Using PROMIS®, Linking PROMIS®