Operative Therapy of Acromioclavicular Joint Seperations Medium- and longterm results after operative therapy of Acromioclavicular Joint Dislocations with a hookplate

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00009446

Enrollment

100

Registered

2016-05-09

Start date

2016-10-21

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

S43.1

Interventions

Group 1: The objective of the study is the retrospective assesment of the functional outcome after AC-joint-dislocations with following operative therapy: Repositioning of the joint with a hookplate(f

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: operative therapy of an AC-Luxation with a hookplate at the BGU Tübingen

Exclusion criteria

Exclusion criteria: patient does not want to participate patient cannot be examined or interviewed

Design outcomes

Primary

Measure	Time frame
The primary outcome is to assess the functional outcome of the applied therapy. The Trial includes an extended clinical examination and consultation of the patients. This will be done in the context of a regular consultation-hour. The data is to be assesed according to the DASH-Score (Disability of arm, shoulder and hand), the Constant Score, the SF-36 Score (which assesses the patients subjective perception in everyday situations and the patients experiences of pain or lack thereof), the Visual Analog Scale (VAS) and a survey created for this study that gathers various parameters. The Primary Outcome is planned with first examination date of at least one year after completing the therapy.	—

Measure

Time frame

The primary outcome is to assess the functional outcome of the applied therapy. The Trial includes an extended clinical examination and consultation of the patients. This will be done in the context of a regular consultation-hour. The data is to be assesed according to the DASH-Score (Disability of arm, shoulder and hand), the Constant Score, the SF-36 Score (which assesses the patients subjective perception in everyday situations and the patients experiences of pain or lack thereof), the Visual Analog Scale (VAS) and a survey created for this study that gathers various parameters. The Primary Outcome is planned with first examination date of at least one year after completing the therapy.

—

Secondary

Measure	Time frame
Longterm effects and complications (Survey). The point of time for the secondary outcome is set for 5 years after completing the therapy.	—

Countries

Germany

Contacts

Public ContactMarkus Gühring

Berufsgenossenschaftliche Unfallklinik Tübingen

mguehring@bgu-tuebingen.de07071 6060

Outcome results

None listed

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