Dual-Loop Target Controlled Infusion in Laparoscopic Cholecystectomy (DLTCI) (DLTCI)
Primary Purpose
Cholecystolithiasis
Status
Completed
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
Dual-loop TCI
manual
Sponsored by
About this trial
This is an interventional supportive care trial for Cholecystolithiasis focused on measuring Dual-Loop TCI, NI, Laparoscopic Cholecystectomy
Eligibility Criteria
Inclusion Criteria:
- require general anesthesia
- expected to last>30 minutes
- 18~90 years
- ASA Ⅰ~Ⅳ level
Exclusion Criteria:
- psychiatric illness
- supraspinal neurological disorders
- cranial neurosurgical procedures
- patients equipped with a pacemaker
Sites / Locations
- Guangzhou Military Region General Hospital, Department of Anesthesiology
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Dual-Loop TCI
manual
Arm Description
the controller in the current study measures and calculates the error(NI error),which is the difference between the set point(NI=36)and the measured NI.If the NI error is different from 0,the controller determines a new propoflo and/or remifentanil concentration.
the investigator modified the effect-site target concentrations of both drugs without minimum or maximum concentration limits without using the Narcotrend monitor only depend on the experience of anesthesiologist.
Outcomes
Primary Outcome Measures
The total dose of propofol and remifentanil
record the total dose of propofol and remifentanil from the beginning to the end of anesthesia.
Secondary Outcome Measures
Full Information
NCT ID
NCT02116985
First Posted
April 15, 2014
Last Updated
April 14, 2015
Sponsor
Guangzhou General Hospital of Guangzhou Military Command
1. Study Identification
Unique Protocol Identification Number
NCT02116985
Brief Title
Dual-Loop Target Controlled Infusion in Laparoscopic Cholecystectomy (DLTCI)
Acronym
DLTCI
Official Title
Dual-Loop Target Controlled Infusion of Propofol and Remifentanil Guided by Narcotrend Index in Laparoscopic Cholecystectomy
Study Type
Interventional
2. Study Status
Record Verification Date
April 2015
Overall Recruitment Status
Completed
Study Start Date
November 2013 (undefined)
Primary Completion Date
October 2014 (Actual)
Study Completion Date
October 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Guangzhou General Hospital of Guangzhou Military Command
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Laparoscopic Cholecystectomy applied to Artificial pneumoperitoneum and the extent of Surgical stimulation cause the wave of hemodynamics increase vigorously, which make it difficult to judge the depth of anesthesia according to traditional hemodynamics index such as heart rate and blood pressure.In case of this, the investigators design this research to study the Closed-Loop Target Controlled Infusion to anaesthesia of individualization guided by a Narcotrend index monitor in Laparoscopic Cholecystectomy.
Detailed Description
Anesthetics alter electrocortical activity in a dose-dependent manner,and it is suggested that electroencephalographic(EEG)activity can provide a reliable basis for a surrogate measurement of hypnosis.An EEG monitor,the Narcotrend Index(NI),has proven useful to titrate hypnotic drugs.Because it is a single composite measure monitored continuously,it has been used in controlled studies to automatically guide propofol administration.Conversely,automated delivery systems for opioids have seldom been described using EEG activity There are no specific measures to quantify analgesia directly.Nevertheless,in the interaction between opioid-hypnotic synergy and loss of consciousness,when the dose of analgesic administered is sufficient to inhibit autonomic response to noxious stimuli,then the required hypnotic concentration is only that needed to achieve loss of consciousness.Moreover,a noxious stimulus such as laryngoscopy or periosteal pressure to the tibia may cause electrocortical activation with an increase in Narcotrend index,which indirectly reflects the analgesic state or the level of antinociception.Finally,an excitatory EEG arousal reaction resulting from nociceptive stimulation can provide a rational basis for analgesia administration.It can then be hypothesized that Narcotrend index could also be the controlled variable for opioid administration.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cholecystolithiasis
Keywords
Dual-Loop TCI, NI, Laparoscopic Cholecystectomy
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
64 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Dual-Loop TCI
Arm Type
Experimental
Arm Description
the controller in the current study measures and calculates the error(NI error),which is the difference between the set point(NI=36)and the measured NI.If the NI error is different from 0,the controller determines a new propoflo and/or remifentanil concentration.
Arm Title
manual
Arm Type
Placebo Comparator
Arm Description
the investigator modified the effect-site target concentrations of both drugs without minimum or maximum concentration limits without using the Narcotrend monitor only depend on the experience of anesthesiologist.
Intervention Type
Device
Intervention Name(s)
Dual-loop TCI
Intervention Description
the controller in the current study measures and calculates the error(NI error),which is the difference between the set point(NI=36)and the measured NI.If the NI error is different from 0,the controller determines a new propoflo and/or remifentanil concentration.
Intervention Type
Device
Intervention Name(s)
manual
Intervention Description
the investigator modified the effect-site target concentrations of both drugs without minimum or maximum concentration limits without using the Narcotrend monitor only depend on the experience of anesthesiologist.
Primary Outcome Measure Information:
Title
The total dose of propofol and remifentanil
Description
record the total dose of propofol and remifentanil from the beginning to the end of anesthesia.
Time Frame
within two hours from the beginning to the end of the propofol and remifentanil
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
require general anesthesia
expected to last>30 minutes
18~90 years
ASA Ⅰ~Ⅳ level
Exclusion Criteria:
psychiatric illness
supraspinal neurological disorders
cranial neurosurgical procedures
patients equipped with a pacemaker
Facility Information:
Facility Name
Guangzhou Military Region General Hospital, Department of Anesthesiology
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510010
Country
China
12. IPD Sharing Statement
Citations:
PubMed Identifier
21233500
Citation
Liu N, Chazot T, Hamada S, Landais A, Boichut N, Dussaussoy C, Trillat B, Beydon L, Samain E, Sessler DI, Fischler M. Closed-loop coadministration of propofol and remifentanil guided by bispectral index: a randomized multicenter study. Anesth Analg. 2011 Mar;112(3):546-57. doi: 10.1213/ANE.0b013e318205680b. Epub 2011 Jan 13.
Results Reference
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Dual-Loop Target Controlled Infusion in Laparoscopic Cholecystectomy (DLTCI)
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