Overview

Dexmedetomidine Facilitate Analgesia

Status:
Completed
Trial end date:
2021-08-03
Target enrollment:
0
Participant gender:
All
Summary
Pre-clinic evidences showed that DEX produces antinociception by inhibiting the activation of spinal microglia and astrocyte decreasing noxious stimuli evoked release of nociceptive substances and further interrupting the spinal neuron-glia cross talk and regulating the nociceptive transmission under chronic pain condition. in this study, the analgesic efficacy of Dexmedetomidine was evaluated by a new non-invasive nociceptive index (qNOX). In this study, Anagel6000 analgesia monitor was used to quantitatively compare the analgesic efficacy of Dexmedetomidine compared with Midazolam.
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
China International Neuroscience Institution
Treatments:
Dexmedetomidine
Midazolam
Criteria
Inclusion Criteria:

- aged from 18 to 80 years old

- American Association of anesthesiologists (ASA) grade Ⅱ ~ IV

- body mass index (BMI) 18.5-40

- planning undergoing peripheral nerve block

Exclusion Criteria:

- incomplete effect of nerve block

- Alzheimer's disease

- implanted cardiac pacemakers

- mental illness

- epilepsy

- autonomic nervous system diseases

- projected the duration of the operation was more than 3 hours