Condition: Postoperative Pain · Sponsor: CSPC Ouyi Pharmaceutical Co., Ltd.
This is a randomized, double-blind, active drug- and placebo-controlled, dose-escalation clinical study conducted in patients scheduled to undergo abdominal surgery. It aims to evaluate the tolerability, safety, pharmacokinetics, and efficacy of SYH9089 Injection for postoperative analgesia in these patients.
This description comes directly from the study's public registry record.
Clinical Trials Information Group officer · 86-0311-69085587 · ctr-contact@cspc.cn
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| The Third Xiangya Hospital of Central South University | Changsha, Hunan, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07519109