Recording of Intraoperative Spinal Cord Stimulation and Monitoring
Recruiting
N/A
Interventional Study
Cervical Stenosis
Disk, Herniated
Spondylosis
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 150 (estimated)
- Sponsor
- University of California, Los Angeles · Other
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About This Trial
Opioid overdose suppresses brainstem respiratory circuits, causes apnea, and may result in death. Epidural electrical stimulation (EES) at the cervical spinal cord facilitated motor activity in rodents and humans, and we hypothesized that EES of the cervical spinal cord could antagonize opioid-induced respiratory depression in humans. In this study, we will stimulate the spinal cord during surgery…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Any patients undergoing brain or spinal cord surgery where spinal neuromonitoring is utilized.
Exclusion Criteria:
* none
Contacts