drugset / Trial / NCT02267681

Opioid Effects on Cognitive Function Following Colonoscopy

NCT02267681

Phase 4 Completed 150 enrolled Perihan Ekmekçi
RandomizedParallel-groupSingle-blind

Summary

This study aims to compare the effects of fentanyl and alfentanil on postprocedural cognitive function in elective endoscopy. 150 patients will be enrolled in the study. Patients meeting eligibility criteria will be randomly allocated to three groups. The patients in Group A will be given propofol and alfentanil. The patients in Group F will be given propofol and fentanyl. Group P is designated as the control group and the patients will be given propofol for sedation. Awareness, vital signs and pain will be evaluated. Side effects will be recorded. Patient and endoscopist satisfaction will be evaluated.

Timeline

Start
2014-10
Primary completion
2016-05
Completion
2016-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Alfentanil Other / unclassified 10 ug/kg Intravenous
Subject Fentanyl Other / unclassified 1 ug/kg Intravenous
Background Propofol Small molecule 100 ug/kg Intravenous