drugset / Trial / NCT07593313

Treatment of Post-Stroke Central Pain

NCT07593313 ↗

Recruiting 80 enrolled Nanchong Central Hospital
RandomizedParallel-groupSingle-blindTreatment

Summary

To evaluate the short-term analgesic efficacy of stSCS combined with pharmacotherapy compared with pharmacotherapy alone in patients with CPSP, measured by Numerical Rating Scale (NRS) score immediately after treatment.

Timeline

Start
2024-01-01
Primary completion
2026-08-01
Completion
2026-08-01

Drugs

EvaluationDrugModalityDoseRoute
Background Amitriptyline Small molecule 25 mg —
Background Amitriptyline Small molecule 75 mg —
Background Duloxetine Small molecule 60 mg —
Background Duloxetine Small molecule 120 mg —
Background Gabapentin Unknown 900 mg —
Background Gabapentin Unknown 1800 mg —
Background Pregabalin Small molecule 150 mg —
Background Pregabalin Small molecule 300 mg —

Indications

No indication recorded.