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Clinical Trials/NCT02890186
NCT02890186
Unknown
Phase 4

Dual-loop Target Controlled Infusion for Coadministration of Propofol and Remifentanil Guided by Narcotrend Index in Anterior Cervical Decompression and Fusion With Internal Fixation

Guangzhou General Hospital of Guangzhou Military Command1 site in 1 country60 target enrollmentApril 2016
ConditionsAnesthesia

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Anesthesia
Sponsor
Guangzhou General Hospital of Guangzhou Military Command
Enrollment
60
Locations
1
Primary Endpoint
the total dose of propofol and remifentanil
Last Updated
9 years ago

Overview

Brief Summary

To investigate the application of closed target-controlled infusion(TCI) of propofol and remifentanil guided by Narcotrend index in the anterior cervical decompression and fusion with internal fixation surgery.

Detailed Description

Sixty patients scheduled for anterior cervical decompression and fusion with internal fixation surgery under general anesthesia were randomly divided into two groups:closed-loop (group A,n=30) and open-loop group(group B,n=30).The procedure during induction of anesthesia was same in two groups.In group A,if Narcotrend index(NI) fall down to 46 and keep more than 30 seconds,propofol and remifentanil were intravenously infused as feedback automatically to achieve the target NI of 26-46.However,the NI in group B was controlled manually.

Registry
clinicaltrials.gov
Start Date
April 2016
End Date
September 2016
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Guangzhou General Hospital of Guangzhou Military Command
Responsible Party
Principal Investigator
Principal Investigator

bo xu

associate chief physician

Guangzhou General Hospital of Guangzhou Military Command

Eligibility Criteria

Inclusion Criteria

  • ASA Ⅰ \~ Ⅱ women undergoing Laparoscopic surgery.
  • Written informed consent from the patient or the relatives of the participating patient.
  • BMI:18.0~25 kg/m2

Exclusion Criteria

  • Mental illness can not match
  • epidural anesthesia contraindicated
  • People who have Slow-type arrhythmias
  • Chronic renal failure
  • Alcohol or drug abuse
  • Already taking gabapentin, pregabalin, benzodiazepin or antidepression drug

Outcomes

Primary Outcomes

the total dose of propofol and remifentanil

Time Frame: within three hours from the beginning to the end of the propofol and remifentanil

record the total dose of propofol and remifentanil from the beginning to the end of anesthesia

Study Sites (1)

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