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Study identifier: NCT07593313 Synced from ClinicalTrials.gov · July 30, 2026
● Recruiting

Treatment of Post-Stroke Central Pain

Condition: Central Post-Stroke Pain  ·  Sponsor: Nanchong Central Hospital

PhaseNA
Planned participants80
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Zhenguo Gao  ·  18404999336  ·  gaozhenguo0822@163.com

Always discuss trial participation with your own doctor first.

Locations (1)

Nanchong Central HospitalNanchong, Sichuan, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT07593313