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Clinical Trial Summary

Blood concentrations of Ciprofol were measured at different time points after single injection in patients with hypoproteinemia


Clinical Trial Description

This study was a single-center, interventional clinical study. Patients with different plasma albumin levels were selected before surgery and induced by a single injection of Ciprofol at a depth of 0.3 mg/kg. 2ml of venous blood was collected before and 0.5, 1, 2, 3, 5, 8, 15, 30min, 1h, 2h and 4h after administration. The pharmacokinetics of Ciprofol were studied by measuring the concentration of Ciprofol in blood. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06425757
Study type Interventional
Source Zhejiang Cancer Hospital
Contact XIE Kangjie, doctoral
Phone 13516721870
Email xiekj@zjcc.org.cn
Status Recruiting
Phase Phase 4
Start date April 1, 2024
Completion date December 30, 2024

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