Comparation Analgesia Efficiency With Propofol Combine Sevoflurane vs Propofol (NCT03841812) | Clinical Trial Compass
CompletedPhase 3
Comparation Analgesia Efficiency With Propofol Combine Sevoflurane vs Propofol
China146 participantsStarted 2020-01-20
Plain-language summary
This study purpose to compare analgesia efficiency of propofol combine with sevoflurane with propofol only using index of Nociception (NOX)
Who can participate
Age range18 Years – 65 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Participants were aged 18-65 years old,
* American Society of Anesthesiologists (ASA) physical status I, II or III
* scheduled to have urological surgery(would last longer than 1 h)
* requiring general anesthesia.
Exclusion criteria:
* refused to participate in this study;
* Unable to communicate normally because of consciousness alterations;
* a history of allergy to opioids
* contraindications to inhalational anesthesia
* a family history of malignant hyperthermia
* a history of alcohol or drug abuse
* received central nervous system-active drugs
* super obese as defined by a body mass index ≥40 kg/m2
* conditions liable to alter the pharmacokinetic and pharmacodynamic behaviors of the intravenous and inhalation anesthetics
* previous head injury
* neurologic
* psychiatric disease
* any disabling central nervous
* cerebrovascular disease
* using psychoactive
* anti-convulsive medications at the time
* unstable angina
* manifested congestive heart failure
* expected difficulty airway management
What they're measuring
1
qNOX change
Timeframe: during operation
Trial details
NCT IDNCT03841812
SponsorChina International Neuroscience Institution