The Reverse shoulder prosthesis as a rivision instrument after failed surgical treatment of proximal humeral fractures using a fracture prosthesis: clinical and radiological medeum-term results

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00012372

Enrollment

Registered

2017-04-28

Start date

2016-10-25

Completion date

Unknown

Last updated

2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

S46.0 S42.21

Interventions

Group 1: Trial participants are examined within a follow-up regarding strengh, mobility und pain measured by use of the ASES- and Constant-Shoulder score respectively a visual analoge pain scale. Radi

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Status post proximal humeral fracture. Status post implantation of a humeral shoulder prosthesis (indication due to the fact that the proximal humerus was fractured). Status post revisionarthoplasty by replacing the anatomical shoulderprothsesis with a reversed prosthesis.

Exclusion criteria

Exclusion criteria: - Omarthosis given as the main indication for implanting a reversed shoulder prosthesis - rheumatoid arthritis - dimentia respectively patients that are incapacitated

Design outcomes

Primary

Measure	Time frame
pain (mesured by showing the patients a visual analogue scale, wich is contained in both the form used to calculate the ASES-score and the Constant-shoulder-score)	—

Secondary

Measure	Time frame
strength, mobility and function of both of the patient's shoulders evaluated by use of the ASES- und the Constant-shoulder-score	—

Countries

Germany

Contacts

Public ContactMirjam Siemes

WWU Münster/ Orthopädische Praxisklinik Münster

m_siem06@uni-muenster.de015751445893

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026