Status:
COMPLETED
SPI-guided vs PRD-guided Analgesia During FESS for Intraoperative Blood Loss
Lead Sponsor:
Medical University of Silesia
Conditions:
Endoscopic Sinus Surgery
Eligibility:
All Genders
18-80 years
Phase:
NA
Brief 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 intraopera...
Detailed Description
Intraoperative blood loss during FESS constitutes a major problem for a surgeon because it influences quality of surgical field. Each incident of haemorrhage makes the operator stop the procedure in o...
Eligibility Criteria
Inclusion
- 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
- age under 18 years old
- allergy to propofol
- pregnancy
- any anatomical malformation making PRD or SE measurement impossible
Key Trial Info
Start Date :
June 1 2016
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
January 15 2018
Estimated Enrollment :
105 Patients enrolled
Trial Details
Trial ID
NCT03389763
Start Date
June 1 2016
End Date
January 15 2018
Last Update
January 26 2018
Active Locations (1)
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1
Medical University of Silesia
Sosnowiec, Silesian Voivodeship, Poland, 41-200