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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