Analgesia Nociception Index-guided Anesthesia and Standard Anesthesia

Not Applicable

Not yet recruiting

• Conditions: Gastric Cancer
• Interventions: Behavioral: Analgesia nociception index-guided anesthesia; Behavioral: Standard anesthesia

• Registration Number: NCT06123637
• Lead Sponsor: Ajou University School of Medicine

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.

Detailed Description

Not available

Study Timeline

• Status Verified: 2023-11
• Study First Submitted: 2023-11-01
• Study First Submitted QC: 2023-11-07
• Last Update Submitted: 2023-11-07
• Study First Posted: 2023-11-09
• Last Update Posted: 2023-11-09
• Study Start: 2024-01-02
• Primary Completion: 2024-12-30
• Study Completion: 2024-12-30

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: All
• Target Recruitment: 68

Inclusion Criteria

• Clinical diagnosis of gastric cancer

Exclusion Criteria

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

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Analgesia nociception index group	Analgesia nociception index-guided anesthesia	-
Standard group	Standard anesthesia	-

Primary Outcome Measures

Name	Time	Method
Remifentanil requirement	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