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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

TypeNameDescription
DRUGEsketamine(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.
DRUGRemifentanil (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.
DRUGFlurbiprofen (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.
DEVICESpinal Cord StimulationCollect resting-state EEG data and NRS scores with the spinal cord stimulator both turned off and on.
OTHERNo interventionCollect 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.