drugset / Trial / NCT06178926

Ciprofol Sedation in Patients Undergoing Liver Cancer Percutaneous Radiofrequency Ablation

NCT06178926

Unknown 80 enrolled Zhejiang Cancer Hospital
RandomizedParallel-groupDouble-blindTreatment

Summary

Efficacy and Safety of Ciprofol Sedation in Patients Undergoing Liver Cancer Percutaneous Radiofrequency Ablation

Timeline

Start
2023-08-01
Primary completion
2024-12-30
Completion
2024-12-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Cipepofol Small molecule 0.2 mg/kg Intravenous
Subject Cipepofol Small molecule 0.3 mg/kg Intravenous
Comparator Propofol Small molecule 1 mg/kg Intravenous
Comparator Propofol Small molecule 2 mg/kg Intravenous

Indications