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.
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Locations near you
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Full eligibility criteria for NCT02890186
Ages eligible for Study
23 Years to 65 Years
Genders eligible for Study
Accepts Healthy Volunteers
ASA Ⅰ ~ Ⅱ women undergoing Laparoscopic surgery.
Written informed consent from the patient or the relatives of the participating patient.
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
All locations for NCT02890186
Guangzhou Military Region General Hospital, Department of Anesthesiology
Guangzhou, Guangdong, China, 510010
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View full eligibility
Tris trial is registered with FDA with number: NCT02890186. The sponsor of the trial is Guangzhou General Hospital of Guangzhou Military Command and it is looking for 60 volunteers for the current phase.
Official trial title: Dual-loop Target Controlled Infusion for Coadministration of Propofol and Remifentanil Guided by Narcotrend Index in Anterior Cervical Decompression and Fusion With Internal Fixation
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