Study of clinical outcome of patients after vertebral body replacement of the ventral thoracal and lumbal spine

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00031452

Enrollment

100

Registered

2023-03-13

Start date

2023-02-06

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

Vertebral body fractures S32.00

Interventions

Group 1: Investigation of clinical outcome of patients after implantation of dorsal stabilization in the lower spine after traumatic vertebral body fracture and vertebral body replacement using data c

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients with fractures in the spine and lumbar spine treated at UMG by ventral spondylodesis with 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
None in the conventional sense; The aim of the study is to follow up the clinical outcome of patients after implantation of a vertebral body replacement in order to ensure an anatomically correct positioning of the spine as far as possible and to eliminate or at least reduce malpositions in order to ultimately improve the treatment of patients!	—

Secondary

Measure	Time frame
Expression of pain symptoms	—

Countries

Germany

Contacts

Public ContactWolfgang Lehmann

Universitätsmedizin Göttingen

wolfgang.lehmann@med.uni-goettingen.de+49 551 396 2462

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 6, 2026