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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04821180
Other study ID # HUMERUS-PSY
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 2016
Est. completion date March 2021

Study information

Verified date March 2021
Source Azienda Ospedaliero-Universitaria Consorziale Policlinico di Bari
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

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.


Recruitment information / eligibility

Status Completed
Enrollment 63
Est. completion date March 2021
Est. primary completion date January 2019
Accepts healthy volunteers No
Gender All
Age group 70 Years and older
Eligibility Inclusion Criteria: - Three and four-part proximal humeral fractures according to Neer classification system; - Patients seventy years or older; - Shoulder surgery within one week after trauma Exclusion Criteria: - Exposed fractures; - Pathological fractures; - Proximal humerus fractures with metaphyseal or diaphyseal extension; - Contraindications to surgery associated with organ dysfunctions or with coagulopathy; - Allergy or hypersensitivity to the orthopedic implants; - Patients who were unable to attend the different follow-ups; - Patients with psychiatric disorders

Study Design


Intervention

Procedure:
Three and four-part proximal humeral fractures' treatment
Open Reduction and Internal Fixation with angle stable plate PHILOS versus RSA (Reverse Shoulder Arthroplasty

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Azienda Ospedaliero-Universitaria Consorziale Policlinico di Bari

Outcome

Type Measure Description Time frame Safety issue
Primary Change in Constant's score The shoulder functionality was quantified using the Constant's score ranging between 0 (most disability) and 100 points (least disability). T0 (one-month), T1 (six months), T2 (one year) post operatively
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®