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

NCT03389763 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 105

Last updated 2018-01-26

No results posted yet for this study

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)

Conditions

  • Endoscopic Sinus Surgery

Interventions

DRUG

Remifentanil

a rate of infusion will be increased by 50% every 5 minutes

Sponsors & Collaborators

  • Medical University of Silesia

    lead OTHER

Principal Investigators

  • Przemysław O Jałowiecki, Ph.Dr · Medical University of Silesia

Study Design

Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

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

Countries

  • Poland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03389763 on ClinicalTrials.gov