Condition: Neuromuscular Blockade · Sponsor: Jiangsu HengRui Medicine Co., Ltd.
The study will enroll adult patients scheduled for elective surgery requiring general anesthesia. Participants will be randomly assigned to receive either HRS-9190 for Injection or Cisatracurium. The primary objective is to measure the duration from cessation of the study drug infusion until the recovery of neuromuscular function to a specific level (TOFr ≥ 90%). Secondary objectives include onset time, duration of action, total time of adequate muscle relaxation during surgery, and neuromuscular recovery pattern.. Safety assessments will include monitoring of adverse events, vital signs, laboratory parameters, and other safety indicators throughout the study period. The hypothesis of this study is that HRS-9190 for Injection could provide effective neuromuscular relaxation, with a satisfied safety profile in the target patient population.
This description comes directly from the study's public registry record.
Lei Tang · +0518-81220121 · lei.tang.lt31@hengrui.com
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| ZhongShan Hospital Fudan University | Shanghai, Shanghai Municipality, China | Recruiting |
| Shanxi Provincial People'S Hospital | Taiyuan, Shanxi, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07446309