Retrospective study of fractures of the coronoid process of the ulna

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00016177

Enrollment

Registered

2019-01-23

Start date

2018-12-01

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

S52.02

Interventions

Group 1: Patients following operative and non-operative treatment of a coronoid ulna- fracture will be investigated for the fragment-size and clinical outcome (range of motion, if applicable Disabilit

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: fractures of the coronoid process of the ulna treatment between 06/01/2011 and 07/31/2018

Exclusion criteria

Exclusion criteria: age below 18 years

Design outcomes

Primary

Measure	Time frame
Aim of the study is the investigation of the fragment size of fractures of the coronoid process and the correlation with the clinical outcome after 6 weeks, 3 or 6 months. Outcome: range of motion, pain (0-10 visual analog scale), subjective satisfaction with clinical result, stability (stable / instable). Additionally measurement of the fragment-size on the ct-scan at the time of injury. end-point: clinical outcome at the last routine-checkup (6 weeks, 3 or 6 month, depending on the last appointment at the clinic)	—

Measure

Time frame

Aim of the study is the investigation of the fragment size of fractures of the coronoid process and the correlation with the clinical outcome after 6 weeks, 3 or 6 months. Outcome: range of motion, pain (0-10 visual analog scale), subjective satisfaction with clinical result, stability (stable / instable). Additionally measurement of the fragment-size on the ct-scan at the time of injury. end-point: clinical outcome at the last routine-checkup (6 weeks, 3 or 6 month, depending on the last appointment at the clinic)

—

Secondary

Measure	Time frame
Aim is the correlation of the fragment size of the fractures with complications occurred during treatment of this injury (non-union, infection, stiffness of the elbow, failure of the osteosynthesis, arthrosis)	—

Countries

Germany

Contacts

Public ContactValentin Rausch

Uniklinik Köln, Klinik für Orthopädie und Unfallchirurgie

valentin.rausch@uk-koeln.de02214780

Outcome results

None listed

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