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Radiological and subjective outcomes following surgical treatment of tibial head fractures

Radiological and subjective outcomes following surgical treatment of tibial head fractures

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00039413
Enrollment
25
Registered
2026-02-20
Start date
2025-07-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

ICD codes S83.53 in conjunction with OPS codes 5-784.7k and 5-784.ek

Interventions

Group 1: Patients who meet the inclusion criteria are identified using the clinic information system and informed by mail (or by telephone, if necessary) about the planned study and the data process

Sponsors

BG Klinikum Duisburg gGmbH
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: •Patients with ACL rupture in combination with a posterolateral tibial head impression fracture type Menzdorf 1b + 1c, 2b + 2c, and 3b •Treatment using ACL reconstruction and arthroscopically assisted transtibial fracture reduction and filling with allogeneic cancellous bone, without the use of additional osteosynthesis material •Written consent to participate in the study

Exclusion criteria

Exclusion criteria: •Accompanying injuries that required additional surgical treatment •Injury to the contralateral knee joint that could influence the outcome •Resection of the anterior cruciate ligament •Posterolateral fracture treatment with osteosynthesis •Non-displaced or minimally displaced posterolateral tibial plateau fractures (Menzdorf type 1a+1b) •Advanced gonarthrosis (Kellgren-Lawrence score >2) •Incomplete documentation in the hospital's internal information system

Design outcomes

Primary

MeasureTime frame
No primary endpoint was defined. For the central question of a satisfactory outcome, the relevant parameters are evaluated purely descriptively and examined to determine the extent to which the results fall within the range of a satisfactory outcome.

Secondary

MeasureTime frame
•Knee function and activity level based on IKDC, Visual Analogue Scale (VAS), ACL-RSI, Tegner Score, and Lysholm Score •Radiological repostitioning results in MRI imaging of the affected knee joint •Re-injury rate •Clinical examination parameters (including mobility, laxity, irritation of the knee)

Countries

Germany

Contacts

Public ContactClaas Neidlein

BG Klinikum Duisburg

Claas.Neidlein@bg-klinikum-duisburg.de+4920376883401

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Aug 10, 2026