Acute and chronic spinal cord disorders requiring surgical decompression.
Conditions
Interventions
Group 1: Single-arm, monocentric, prospective observational study.
Adult patients undergoing surgical spinal cord decompression receive intraoperative, contact-free, contrast-agent-free hyperspectral
Sponsors
Universität Leipzig
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Adult patients (= 18 years) Indication for surgical spinal cord decompression Acute or chronic spinal cord pathology of traumatic, degenerative, inflammatory, or neoplastic origin Ability to provide informed consent Written informed consent for study participation
Exclusion criteria
Exclusion criteria: Minors Pregnancy or breastfeeding Inability to provide informed consent Refusal to participate in the study Emergency surgery without possibility of prior informed consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| WHAT: Change in intraoperative hyperspectral perfusion and oxygenation parameters of the spinal cord WHEN: Intraoperatively at the beginning and end of decompression HOW: Contact-free hyperspectral imaging using a standardized camera system | — |
Secondary
| Measure | Time frame |
|---|---|
| Correlation of intraoperative hyperspectral parameters with preoperative neurological severity and postoperative functional outcome. | — |
Countries
Germany
Contacts
Public ContactJohannes Wach
Universität Leipzig
Outcome results
None listed