Status:
UNKNOWN
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 utility of Pupillary Dilatation Reflex (PRD) for monitoring pain perception intraoperatively and its influence on intraoperative blood loss, quality o...
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 general 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 :
September 1 2021
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
January 15 2023
Estimated Enrollment :
120 Patients enrolled
Trial Details
Trial ID
NCT03417206
Start Date
September 1 2021
End Date
January 15 2023
Last Update
October 22 2020
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