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Clinical Trials/NCT06123637
NCT06123637
Not yet recruiting
Not Applicable

Comparison of Analgesia Nociception Index-guided Anesthesia and Standard Anesthesia on Remifentanil Requirement in Desflurane Anesthesia

Ajou University School of Medicine0 sites68 target enrollmentJanuary 2, 2024
ConditionsGastric Cancer

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Gastric Cancer
Sponsor
Ajou University School of Medicine
Enrollment
68
Primary Endpoint
Remifentanil requirement
Status
Not yet recruiting
Last Updated
2 years ago

Overview

Brief 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.

Registry
clinicaltrials.gov
Start Date
January 2, 2024
End Date
December 30, 2024
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Ajou University School of Medicine
Responsible Party
Principal Investigator
Principal Investigator

Ji Eun Kim

Assistant professor

Ajou University School of Medicine

Eligibility Criteria

Inclusion Criteria

  • Clinical diagnosis of gastric cancer

Exclusion Criteria

  • Conversion to open laparotomy
  • Prior opioid abuse
  • Prior infection
  • Cardiac arrythmia

Outcomes

Primary Outcomes

Remifentanil requirement

Time Frame: at time of the end of skin suture (up to 4 hours)

Assessing the total dose of remifentanil administered from skin incision until skin suture

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