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

• Status: Completed
• Trial end date: 2018-01-15
• Target enrollment: 0
• Participant gender: All

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)

• Phase: N/A
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Medical University of Silesia
• Treatments: Remifentanil

Criteria

Inclusion Criteria:

• written consent to participate in the study

• written consent to undergo functional endoscopic sinus surgery under total intravenous anaesthesia

• ASA (American Society of Anesthesiologists) I-III

Exclusion Criteria:

• age under 18 years old

• allergy to propofol

• pregnancy

• any anatomical malformation making PRD or SE measurement impossible