Geneva, Feb. 13 -- International Clinical Trials Registry received information related to the study (ChiCTR2600118173) titled 'Central venous administration of fospropofol reduces paresthesia: A randomized controlled trial' on Feb. 3.
Study Type: Interventional study
Study Design:
Parallel
Primary Sponsor: The Third People's Hospital of Yibin
Condition:
None
Intervention:
Peripheral vein group:Intravenously administered with fospropofol through the peripheral vein.
Recruitment Status: Not Recruiting
Phase: N/A
Date of First Enrollment: 2026-02-03
Target Sample Size: Peripheral vein group:47;Central venous group:46;
Countries of Recruitment:
China
To know more, visit https://www.chictr.org.cn/showproj.html?proj=292523
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