drugset / Trial / NCT02314559

A Psychomotor Recuperation Study After Deep Sedation for Colonoscopy Between Target Controlled and Manual Titration of Propofol

NCT02314559 ↗

Phase 4 Completed 164 enrolled Brugmann University Hospital
RandomizedParallel-groupTriple-blindSupportive care

Summary

Deep sedation with propofol for ambulatory colonoscopy has become standard clinical practice.To achieve the necessary (e.g.: no excessive movement and no awareness) level of sedation during colonoscopy, propofol can be titrated by hand, continuous infusion or by target controlled infusion. The aim of the investigators is to evaluate sedation efficacy and recovery between two groups of ambulatory patients having a colonoscopy: one group will receive a manual titration of propofol, the other group a target controlled infusion (TCI) of propofol. The investigators will evaluate both groups before, during and after colonoscopy for adverse events, quality of sedation and recovery. When patients are estimated to be ready for discharge, they will also be subjected to a cognitive and a psychomotoricity test.

Timeline

Start
2015-02
Primary completion
2020-07-07
Completion
2020-07-07

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Propofol Small molecule 2 ug/ml —
Subject Propofol Small molecule 6 ug/ml —
Subject Propofol Small molecule 20 mg —
Subject Propofol Small molecule 50 mg —
Subject Propofol Small molecule 400 mg —

Indications

No indication recorded.