Humeral Fracture, Proximal Clinical Trial
Official title:
Angle Stable Plate Versus Reverse Shoulder Treatment for Proximal Humeral Fractures: Should the Psychological Health Influence the Choice of Device
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 |
Verified date | March 2021 |
Source | Azienda Ospedaliero-Universitaria Consorziale Policlinico di Bari |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
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.
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 |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Azienda Ospedaliero-Universitaria Consorziale Policlinico di Bari |
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 |
Status | Clinical Trial | Phase | |
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Completed |
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