drugset / Trial / NCT06409104

Propofol Versus Dexmedetomidine for Sedation of Cancer Patients Undergoing ERCP

NCT06409104 ↗

Completed 202 enrolled National Cancer Institute, Egypt
RandomizedParallel-groupDouble-blindSupportive care

Summary

The aim of this study is to compare the efficacy and safety of propofol and dexmedetomidine during ERCP regarding hemodynamic, respiratory, sedative and cognitive functions.

Timeline

Start
2023-09-01
Primary completion
2024-01-01
Completion
2024-02-01

Drugs

EvaluationDrugModalityDoseRoute
Comparator Dexmedetomidine Other / unclassified 0.2 ug/kg —
Comparator Dexmedetomidine Other / unclassified 0.7 ug/kg —
Comparator Propofol Small molecule 0.05 mg/kg Intravenous
Comparator Propofol Small molecule 0.1 mg/kg Intravenous

Indications

No indication recorded.