Pain Clinical Trial
Official title:
Investigation of the Effect of Opioid Titration Guided by Analgesia Indices During General Anesthesia
This prospective randomized clinical trial evaluates the effects of a monitor-guided opioid analgesia during general anesthesia. To date no standard-monitoring device exists to specifically reflect the analgesic component of general anesthesia. Quality and safety of general anesthesia are of major clinical importance and should be improved by limiting the opioid analgesic's dosage to the minimum amount needed. The study compares the effects of monitoring nociception during general anesthesia with different innovative techniques in comparison to routine clinical practice.
This prospective randomized clinical study aims to investigate the effects of a
monitor-guided opioid analgesia during general anesthesia by different monitoring systems in
comparison to routine clinical practice. Many surgical procedures require general anesthesia.
The main components of general anesthesia are hypnosis and analgesia, and anesthesiologists
usually combine a hypnotic drug with an opioid analgesic.
Until today, however, there is no standard-monitoring of nociception to specifically reflect
the analgesic component of general anesthesia. In clinical practice the opioid dosage is
chosen by clinical judgment of the attending anesthesiologist based upon changes of heart
rate, blood pressure, pupil size, lacrimation and sweating of the patient.
On the one hand, underdosage of opioids can cause nociception leading to an increased
sympathetic tone, increase of plasma levels of stress hormones, nociceptive movements as well
as increase postoperative pain. On the other hand, overdosage of opioids can lead to drug
side effects such as nausea and vomiting, hemodynamic instability, an increase in recovery
times, immunosuppression and an increase in postoperative pain by
opioid-induced-hyperalgesia. Quality and safety of general anesthesia are of major clinical
importance and can be improved by limiting the administration of opioid analgesics to the
optimal individual dose needed. In the last years, different analgesia monitoring devices
have been developed for monitoring nociception. The present study evaluates the effects of
the administration of opioids during general anesthesia guided by three different monitoring
systems in comparison to routine clinical practice. After institutional approval by the
Ethics committee of the Medical Board of the City of Hamburg, Germany and obtaining patients'
written informed consent the investigators randomize elective patients with major abdominal
surgery for open radical prostatectomy into one of four treatment groups.
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