Trials / Not Yet Recruiting
Not Yet RecruitingNCT06531837
Electroencephalographic Characteristics of Chronic Pain in Patients With Spinal Cord Injury
Electroencephalographic Characteristics of Chronic Pain in Patients With Spinal Cord Injury: an Exploratory, Interventional, Non-randomized Controlled Study
- Status
- Not Yet Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 60 (estimated)
- Sponsor
- Beijing Tiantan Hospital · Academic / Other
- Sex
- All
- Age
- 18 Years – 65 Years
- Healthy volunteers
- Not accepted
Summary
The diagnosis of chronic pain currently lacks objective and quantifiable biomarkers. This study aims to observe the EEG characteristics of patients with chronic pain following spinal cord injury and subsequently administer analgesic interventions with remifentanil, esketamine, flurbiprofen, and spinal cord stimulation. The correlation between EEG features and pain intensity will be examined. The research aims to advance the objectification of chronic pain diagnosis and treatment.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Esketamine(Continuous infusion) | Continuous intravenous infusion of esketamine at a dose of 0.2 mg/(kg · h). Collect resting-state EEG data and NRS scores 40 minutes after administration. |
| DRUG | Remifentanil (Target-Controlled Infusion) | The plasma drug concentrations of remifentanil were set at 0.5 ng/ml, 1 ng/ml, and 1.5 ng/ml. After each plasma drug concentration reached a steady state, the NRS scores were assessed, and resting-state EEG was recorded for at least 5 minutes. |
| DRUG | Flurbiprofen (Single intravenous injection) | Single intravenous injection of Flurbiprofen at a dose of 100 mg. Collect resting-state EEG data and NRS scores 10 minutes after administration. |
| DEVICE | Spinal Cord Stimulation | Collect resting-state EEG data and NRS scores with the spinal cord stimulator both turned off and on. |
| OTHER | No intervention | Collect resting-state EEG data and NRS scores. |
Timeline
- Start date
- 2024-08-25
- Primary completion
- 2026-01-31
- Completion
- 2026-02-28
- First posted
- 2024-08-01
- Last updated
- 2024-08-13
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT06531837. Inclusion in this directory is not an endorsement.