Study on the clinical outcome of patients with ventral fusion of the spine using vertebral body replacement, autologous iliac crest or cage implantation

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00034251

Enrollment

300

Registered

2024-05-13

Start date

2019-11-06

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

S22.00

Interventions

Group 1: Patients with traumatic injuries to the spine

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: - Patients with fractures in the area of the thoracic spine and lumbar spine who were treated monosegmentally in the UMG by ventral spondylodesis with cage implantation or autologous pelvic chipplasty - Patients with fractures in the area of the thoracic and lumbar spine who were treated in the UMG with an anterolateral bisegmental vertebral body replacement

Exclusion criteria

Exclusion criteria: - Follow-up of less than 1 year - Patients with pathological or degenerative fractures - Implantations in the area of the cervical spine

Design outcomes

Primary

Measure	Time frame
Analysis of the clinical outcome of three established surgical procedures, i.e. vertebral body replacement, cage implantation and autologous pelvic chipplasty, in the thoracic and lumbar spine	—

Countries

Germany

Contacts

Public ContactKatharina Blanka Jäckle

Universitätsmedizin Göttingen

katharina.jaeckle@med.uni-goettingen.de+495513962462

Outcome results

None listed

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