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Clinical Trials/DRKS00011581
DRKS00011581Completed未知

Clinical, functional and psychosocial outcome of reverse shoulder arthroplasty - a prospective randomized comparison of two types of prostheses after traumatic fracture of the proximal humerus - CEUS #Delta

Zentrum für Orthopädie, Unfallchirurgie und Paraplegiologie0 sites66 target enrollmentStarted: January 18, 2017Last updated:
Conditions

Trial Snapshot

Phase
未知
Status
Completed
Sponsor
Enrollment
66

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional
Allocation
Randomized controlled study
Masking
Open (masking not used)

Eligibility Criteria

Ages
18 Years to one (—)
Sex
All

Inclusion Criteria

  • Patients with multifragmentary fracutres of the proximal humerus and indication of RSA. Patients with rotator cuff arthropathy and indication of planned RSA.

Exclusion Criteria

  • - known intolerance for SonoVue
  • - severe heart failure (NYHA III/IV)
  • - myocardial infarction within the last 14 days
  • - severe respiratory diseases
  • - pregnancy and breastfeeding
  • - age under 18 years

Investigators

Sponsor
Zentrum für Orthopädie, Unfallchirurgie und Paraplegiologie

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