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Clinical Trials/NCT02323958
NCT02323958
Completed
Not Applicable

Effect of Transcutaneous Electrical Acupoint Stimulation on Outcome During Emergence From Anesthesia in Patients Undergoing Robotic Laparoscopic Gynecologic Surgery

Air Force Military Medical University, China1 site in 1 country150 target enrollmentDecember 2014
ConditionsAnesthesia

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Anesthesia
Sponsor
Air Force Military Medical University, China
Enrollment
150
Locations
1
Primary Endpoint
Time to awake
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

This study is to observe whether transcutaneous electrical stimulation at specific acupoints could improve the quality of emergence in patients undergoing robotic laparoscopic gynecologic surgery.

Detailed Description

During robotic laparoscopic gynecologic surgery, the patients are put in an extremely trendelenburg positon. And a long duration of this position could lead to delayed emergence or agitation. Stimulation at some acupoints were reported to improve homeostasis. In this study we tend to observe whether transcutaneous electrical stimulation at specific acupoints could improve the quality of emergence in patients undergoing robotic laparoscopic gynecologic surgery.

Registry
clinicaltrials.gov
Start Date
December 2014
End Date
December 2016
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Air Force Military Medical University, China
Responsible Party
Principal Investigator
Principal Investigator

Zhihong LU

Dr

Air Force Military Medical University, China

Eligibility Criteria

Inclusion Criteria

  • Patients scheduled for robotic laparoscopic gynecologic surgery under general anesthesia
  • Patients with written informed consent

Exclusion Criteria

  • Patients with difficulty in communication
  • Patients with disease of central nervous system

Outcomes

Primary Outcomes

Time to awake

Time Frame: from end of inhaling sevoflurane to departing from postanesthesia care unit(PACU),an anticipated average of 1 hour

time to open eyes to verbal command

Secondary Outcomes

  • PONV(from arriving at PACU to departing from PACU,an anticipated average of 30min)
  • Richmond Score(from end of inhaling sevoflurane to departing from PACU,an anticipated average of 1 hour)
  • QoR-15(from end of inhaling sevoflurane to 24h after surgery,an anticipated average of 24 hour)
  • VAS score(from arriving at PACU to departing from PACU,an anticipated average of 30min)
  • Time to extubation(from end of inhaling sevoflurane to departing from PACU,an anticipated average of 1 hour)
  • serum MMP9(from before anesthesia to after surgery, an anticipated average of 4 hours)
  • residual sedation(from arriving at PACU to departing from PACU,an anticipated average of 30min)
  • serum Aquaporin 4(from before anesthesia to after surgery, an anticipated average of 4 hours)
  • serum S100β(from before anesthesia to after surgery, an anticipated average of 4 hours)

Study Sites (1)

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