Overview
Dexmedetomidine Facilitate Analgesia
Status:
Completed
Completed
Trial end date:
2021-08-03
2021-08-03
Target enrollment:
0
0
Participant gender:
All
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 4Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
China International Neuroscience InstitutionTreatments:
DexmedetomidineMidazolam
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