drugset / Trial / NCT02447796

Dexmedetomidine and Propofol As Sole Sedative Agent for Patients Undergoing Arteriovenous Fistula Surgery

NCT02447796 ↗

Phase 4 Unknown 48 enrolled Baskent University
RandomizedParallel-groupDouble-blindTreatment

Summary

The investigators designed a prospective randomized study to compare the conventionally used sedative drug propofol with a latest alternative dexmedetomidine (DEX), in patients with end-stage renal disease undergoing arteriovenous fistula (AVF) surgery.

Timeline

Start
2015-05
Primary completion
2015-05
Completion
2015-07

Drugs

EvaluationDrugModalityDoseRoute
Comparator Dexmedetomidine Other / unclassified 1 ug/kg —
Comparator Dexmedetomidine Other / unclassified 1.5 ug/kg —
Comparator Propofol Small molecule 1 mg/kg —
Comparator Propofol Small molecule 1.5 mg/kg —