Adequacy of Anaesthesia for Colonoscopic Procedures

• Status: Completed
• Trial end date: 2020-01-31
• Target enrollment: 0
• Participant gender: All

Summary

The aim of this randomized prospective trial is to assess the utility of Adequacy of Anaesthesia technique (Response Entropy and Surgical Pleth Index) for monitoring pain perception intraoperatively and its influence on postoperative pain perception, both patients' and operators' satisfaction in patients undergoing colonoscopic procedures under intravenous sedation using propofol and fentanyl.

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

Details

• Lead Sponsor: Medical University of Silesia
• Treatments: Anesthetics; Fentanyl; Propofol

Criteria

Inclusion Criteria:

• written consent to participate in the study

• written consent to undergo deep sedation for colonoscopic procedure

• general heath condition I-III of American Society of Anaesthesiology

Exclusion Criteria:

• necessity of administration of vasoactive drugs influencing SPI monitoring

• pregnancy

• anatomical malformation that make monitoring using SE sensor impossible

• general atherosclerosis, heart rhythm disturbances impairing SPI monitoring

• chronic medication using opioid drugs leading to resistancy to opioids.