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Trial Title:
Analgesia Nociception Index-guided Anesthesia and Standard Anesthesia
NCT ID:
NCT06123637
Condition:
Gastric Cancer
Conditions: Official terms:
Stomach Neoplasms
Anesthetics
Study type:
Interventional
Study phase:
N/A
Overall status:
Not yet recruiting
Study design:
Allocation:
Randomized
Intervention model:
Parallel Assignment
Primary purpose:
Prevention
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Intervention:
Intervention type:
Behavioral
Intervention name:
Analgesia nociception index-guided anesthesia
Description:
Maintaining the blood pressure based on analgesia nociception index of >50 value
Arm group label:
Analgesia nociception index group
Intervention type:
Behavioral
Intervention name:
Standard anesthesia
Description:
Maintaining the blood pressure based on anesthesiologist's decision
Arm group label:
Standard group
Summary:
The primary purpose of this study is to compare the analgesia nociception index-guided
anesthesia and standard anesthesia on remifentanil requirement in desflurane anesthesia.
Criteria for eligibility:
Criteria:
Inclusion Criteria:
- Clinical diagnosis of gastric cancer
Exclusion Criteria:
- Conversion to open laparotomy
- Prior opioid abuse
- Prior infection
- Cardiac arrythmia
Gender:
All
Minimum age:
20 Years
Maximum age:
85 Years
Healthy volunteers:
No
Start date:
January 2, 2024
Completion date:
December 30, 2024
Lead sponsor:
Agency:
Ajou University School of Medicine
Agency class:
Other
Source:
Ajou University School of Medicine
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT06123637
