Reversed Hill-Sach-Lesion after posterior shoulder dislocation: therapies and results

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00008733

Enrollment

Registered

2015-06-16

Start date

2012-07-01

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

S43.0 S42.2

Interventions

Group 1: Prospective data capture of functional outcomes after surgical treatment of reversed Hill - Sachs lesions using various subjective and objective functional scores.

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: posterior shoulder dislocation and reversed hill-sachs lesion

Exclusion criteria

Exclusion criteria: -Patient's age <18 years -Additional bony injury of the proximal humerus

Design outcomes

Primary

Measure	Time frame
The stability , mobility and function of the shoulder is evaluated using the Constant score questionnaire and the Rowe Score questionnaire. These questionnaires are collected after one year and after 4 years.	—

Secondary

Measure	Time frame
Quality of life was evaluated using the DASH questionnaire score and the subjective perception of pain by the visual analog scale. The data are collected after one year and after 4 years .	—

Countries

Germany

Contacts

Public ContactPatrick Ziegler

BG Unfallklinik Tübingen

pziegler@bgu-tuebingen.de07071/606-3971

Outcome results

None listed

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