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Bilateral arcocristectomy in cervical spinal stenosis via a unilateral, minimally invasive approach with a tubular system

Bilateral arcocristectomy in cervical spinal stenosis via a unilateral, minimally invasive approach with a tubular system

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00016857
Enrollment
10
Registered
2019-02-25
Start date
2019-03-01
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 of age with cervical spinal canal stenosis who underwent bilateral arcocristectomy via a unilateral, minimally invasive approach using a tubular system during the period f

Sponsors

Universitätsklinikum Freiburg
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients = 18 years of age with cervical spinal canal stenosis who underwent bilateral arcocristectomy via a unilateral, minimally invasive approach using a tubular system during the period from 2010 to 09/2018.

Exclusion criteria

Exclusion criteria: Age of the patient < 18 years.

Design outcomes

Primary

MeasureTime frame
Major complications within 30 days after arcocristectomy: death, myocardial infarction, vertebral injury, insult, pulmonary embolism, severe pneumonia with respiratory obligation, re-operation, new motor deficit KG = 3/5, worsening of myelopathy. Occurrence of complications in the further postoperative course (e.g. revision operations)

Secondary

MeasureTime frame
Minor complications within 30 days after arcocristectomy: New motor deficit KG > 3/5, sensitive deficit, mild pneumonia with transient oxygen dependence, postoperative confusion, urinary tract infection, anemia requiring transfusion, deep vein thrombosis, dural tear / liquor fistula. Wound healing disorder. Enlargement of the spinal canal in the operated segment or segments compared to preoperative imaging.

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