UnknownNot Applicable

SPI-guided Analgesia During FESS for Intraoperative Blood Loss

Poland120 participantsStarted 2018-09-01

Plain-language summary

The aim of this randomized trial is to assess the utility of Surgical Pleth Index (SPI) for monitoring pain perception intraoperatively and its influence on intraoperative blood loss, quality of surgical field using Boezaart Bleeding Scale (BBS) in patients undergoing functional sinus surgery (FESS) under total intravenous anaesthesia using propofol or volatile anaesthesia using sevoflurane or desflurane

Who can participate

Age range18 Years – 80 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * written consent to participate in the study * written consent to undergo functional endoscopic sinus surgery under general anaesthesia * ASA (American Society of Anesthesiologists) I-III Exclusion Criteria: * age under 18 years old * allergy to propofol * pregnancy * any anatomical malformation making SE measurement impossible * necessity of administration of vasoactive drugs

What they're measuring

blood loss postoperatively

Timeframe: end of operation,' assessment

Trial details

NCT IDNCT03417180

SponsorMedical University of Silesia

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2023-07-15

Contact for this trial

Michał J Stasiowski, MD

696797922 mstasiowski.anest@gmail.com

View on ClinicalTrials.gov More Endoscopic Sinus Surgery trials