Clinical Trial: Clinical Research Protocol for Comparing the Efficacy of Daytime and Nighttime Target-Controlled Infusion of Propofol Combined with Dexmedetomidine Pump Injection in Patients with Sleep Disorders (China)

China, Aug. 27 -- The Chinese Clinical Trial Registry (ChiCTR) received information related to the study titled 'Clinical Research Protocol for Comparing the Efficacy of Daytime and Nighttime Target-Controlled Infusion of Propofol Combined with Dexmedetomidine Pump Injection in Patients with Sleep Disorders'. The following are the other relevant details related to the trial:

Registration Number: ChiCTR2600130902

Registration Time: 2026/08/26

Type: Interventional study

Primary Sponsor: Xi’an Daxing Hospita

To know more, click on https://www.chictr.org.cn/showprojEN.html?proj=339949

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