Clinically retrospective comparison of ligamentary refixation in elbow instability with and without internal bracing - Pilot study of case number determination

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00012812

Enrollment

Registered

2019-11-18

Start date

2018-05-03

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

S53.3

Interventions

Group 1: Patients whose elbow instability has been refixed by anchor only will be invited for follow-up. At one-time clinical follow-up after at least 12 months and a maximum of 4 years after surgery,

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: -Men and women with completed 18.Lebensjahr -operative treatment of elbow instability with and without internal bracing in DIAKOVERE Friederikenstift -Minimum follow-up 12 months -Maximum follow-up 4 years

Exclusion criteria

Exclusion criteria: - Diseases or injuries that affect arm strength or elbow function -Immunosuppressive therapy

Design outcomes

Primary

Measure	Time frame
The primary goal is to record the range of motion in extension and flexion.	—

Secondary

Measure	Time frame
The secondary goal is to assess stability using an ultrasound scan for humeral-radial deployment.	—

Countries

Germany

Contacts

Public ContactYvonne Noll

Orthopädische Klinik der Medizinischen Hochschule Hannover im Diakovere Annastift, Leitung Klinisches Studienmanagement

yvonne.noll@diakovere.de0511-5354-649

Outcome results

None listed

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