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Subjective neurosurgical evaluation of cervical spine synthetic *BoneMRI* CTs generated with convolutional neural networks.

Subjective neurosurgical evaluation of cervical spine synthetic *BoneMRI* CTs generated with convolutional neural networks. - BoneMRI in Neurosurgical workflow

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON49245
Enrollment
20
Registered
2021-04-22
Start date
2021-07-05
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Cervical radiculopathy neck hernia

Interventions

None listed

Sponsors

Isala Klinieken
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: • Patients with the clinical diagnosis of cervical radiculopathy and/or myelopathy; • Received a MRI cervical spine; • Eligible for cervical spine surgery based on neurosurgical evaluation of the clinical symptoms and imaging.

Exclusion criteria

Exclusion criteria: • History of osteosynthesis in the spine • Previous participation in the study; • Malignancy.

Design outcomes

Primary

MeasureTime frame
The primary outcome is the satisfaction and certainty of the neurosurgeon in the surgery planning measured with a 10-point Likert scale before viewing the BoneMRI preoperative, after viewing the BoneMRI preoperative and postoperative. Comparison of Likert-scores of part A (T0) of the questionnaire to part B (T1) and part A (T0) to part C (T2) will be performed. For the questions of part B and C only pertaining to the BoneMRI, the median or mean Likert scores of each question, depending on normality of the data, is evaluated.

Secondary

MeasureTime frame
The secondary outcome is the diagnostic accuracy of BoneMRI in visualization of pathoanatomic aspects related to radiculopathy compared to the current workflow (MRI, X-ray and CT scan if available) as assessed by the neurosurgeon with perioperative findings serving as reference standard.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)