drugset / Trial / NCT03389763

SPI-guided vs PRD-guided Analgesia During FESS for Intraoperative Blood Loss

NCT03389763

Completed 105 enrolled Medical University of Silesia
RandomizedParallel-groupSingle-blindDiagnostic

Summary

The aim of this randomized trial is to assess the efficacy of analgesia , compare the utility of Pupillary Dilatation Reflex (PRD), Surgical Pleth Index (SPI) for monitoring pain perception intraoperatively and their influence on intraoperative blood loss, quality of surgical field using Boezaart Bleeding Scale (BBS) in patients undergoing functional sinus surgery (FESS)

Timeline

Start
2016-06-01
Primary completion
2018-01-15
Completion
2018-01-15

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Remifentanil Small molecule 0.25 ug/kg Intravenous

Indications

No indication recorded.