Trials / Recruiting
RecruitingNCT05356286
Recording of Intraoperative Spinal Cord Stimulation and Monitoring
- Status
- Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 150 (estimated)
- Sponsor
- University of California, Los Angeles · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
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 and assess its effects on respiratory function in human patients.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | epidural electrical stimulation | Electrical spinal cord stimulation will be used to modulate respiratory function during general anesthesia. |
Timeline
- Start date
- 2011-01-21
- Primary completion
- 2027-01-22
- Completion
- 2027-01-22
- First posted
- 2022-05-02
- Last updated
- 2025-03-10
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT05356286. Inclusion in this directory is not an endorsement.