S42.2
Conditions
Interventions
Group 1: Patients who are treated by wearing a new type of shoulder orthosis with hypomochlion and in internal rotation.
Allocation to this study arm is randomized by lot (opaque, unlabeled envelope,
lateral), recording of outcomes
Day 7: X-ray in 2 planes (a.p.
lateral), recording of outcomes
Day 7: X-ray in 2 planes (a
Sponsors
Klinikum der LMU München, Muskuloskelettales Universitätszentrum München
Eligibility
Sex/Gender
All
Age
18 Years to 90 Years
Inclusion criteria
Inclusion criteria: -Diagnosis of a recent (maximum interval between trauma and diagnosis 2 weeks), previously untreated proximal humerus fracture -Voluntary verbal and written consent to participate in the study only by patients by patients who are able to give their consent themselves
Exclusion criteria
Exclusion criteria: - Serious concomitant diseases that could impair rehabilitation - Previous operations or injuries to the affected extremity - Inability to fulfill the requirements of the study - Pregnancy - Known mental illness that could affect participation in the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Completion of a standardized questionnaire using PROMS | — |
Secondary
| Measure | Time frame |
|---|---|
| Radiological measurement of the CCD, LHO, LSA, DSA using X-ray a.p. and laterally, conversion to surgical therapy | — |
Countries
Germany
Contacts
Public ContactKatharina Kirchhoff
Klinikum der LMU München, Muskuloskelettales Universitätszentrum München
Outcome results
None listed