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Posterior decompression and fusion in patients with multi-level cervical spondylotic myelopathy

Posterior decompression and fusion in patients with multi-level cervical spondylotic myelopathy

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00014285
Enrollment
100
Registered
2018-03-14
Start date
2018-01-01
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

M47.12

Interventions

Group 1: Patients = 18 years with degenerative, multi-level, cervical spondylotic myelopathy surgically treated with multi-level posterior decompression and fusion over the period of 2004-2016. The po

Sponsors

Universitätsklinikum Freiburg
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients = 18 years with multi-level cervical spondylotic myelopathy treated surgically with multi-level posterior decompression and fusion over the period 2004-2016.

Exclusion criteria

Exclusion criteria: Patients <18 years. For measurement of cervical range of motion in outpatient examination: Uncooperative patients; Patients who can not sit on an examination chair due to other physical limitations; Patient with pacemaker and defibrillator.

Design outcomes

Primary

MeasureTime frame
Major complications occuring within 30 days after posterior decompression and fusion in patients with multi-level cervical spondylotic myelopathy: death, myocardial infarction, vertebral artery injury, insult, pulmonary embolism, severe pneumonia with respiratory care, reoperation, new motor deficit KG = 3/5. Incidence of complications in the further postoperative course (e.g., revision surgery). The postoperative complications are retrospectively collected from medical records. Current Cervical Spine Disorders / Pain on the numeric rating scale (NRS). The current complaints are collected in the outpatient clinic or via questionnaires or telephone interviews. Objective measurement of parameters of cervical spine mobility (inclination, reclination, lateral tilt, and rotation). For the objective measurement, a non-invasive measuring device (CROM3, Performance Attainment Associates), which has already been validated in several studies, is used.

Secondary

MeasureTime frame
Minor complications occurring within 30 days after posterior decompression and fusion in patients with multi-level cervical spondylotic myelopathy: new motor deficit KG> 3/5, mild pneumonia with transient oxygen demand, postoperative confusion, urinary tract infection, transfusion-dependent anemia, deep vein thrombosis, hepatic insufficiency, dural lesion / CSF fistula. The postoperative complications are retrospectively collected from medical records. Subjective restriction of movement, information on quality of life and impairment in everyday life (e.g. driving), patient satisfaction. The current complaints are collected in the outpatient clinic or via questionnaires or telephone interviews.

Countries

Germany

Contacts

Public ContactChristoph Scholz

Klinik für Neurochirurgie Universitätsklinikum Freiburg

christoph.scholz@uniklinik-freiburg.de076127050010

Outcome results

None listed

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