M19.01
Conditions
Interventions
Group 1: Patients assigned to the CPM group begin therapy on the second postoperative day (once daily during their hospital stay) and, following inpatient treatment, are provided with a CPM unit on lo
Sponsors
Herz-Jesu-Krankenhaus Münster-Hiltrup
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: All patients undergoing elective implantation of a reverse prosthesis at the study center are included. Indications include cuff tear arthropathy, primary glenohumeral osteoarthritis, and post-traumatic conditions.
Exclusion criteria
Exclusion criteria: Patients with fractures, infections, rheumatic diseases, local tumors, and revision procedures involving the affected shoulder.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Constant-Score: Assessed via standardized questionnaire and clinical examination after four weeks (at the end of home-based CPM treatment), and again at three and six months. A final examination takes place after one year (according to the literature, no further improvement is to be expected between the first and second year following the implantation of a reverse prosthesis). | — |
Secondary
| Measure | Time frame |
|---|---|
| Outcome scores (ASES, DASH, SANE, OSS) and ranges of motion Data collected via standardized questionnaire and clinical examination at four weeks (end of home-based CPM treatment) and at three and six months. A final examination takes place after one year (according to the literature, no further improvement is to be expected between the first and second year following implantation of a reverse prosthesis). | — |
Countries
Germany
Contacts
Public ContactBenedikt Schliemann
Herz-Jesu-Krankenhaus Münster-Hiltrup
Outcome results
None listed