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The primary purpose of this study is to compare the analgesia nociception index-guided anesthesia and standard anesthesia on remifentanil requirement in desflurane anesthesia.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Analgesia nociception index group | Experimental |
| |
| Standard group | Placebo Comparator |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Analgesia nociception index-guided anesthesia | Behavioral | Maintaining the blood pressure based on analgesia nociception index of >50 value |
|
| Measure | Description | Time Frame |
|---|---|---|
| Remifentanil requirement | Assessing the total dose of remifentanil administered from skin incision until skin suture | at time of the end of skin suture (up to 4 hours) |
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Inclusion Criteria:
Exclusion Criteria:
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| ID | Term |
|---|---|
| D013274 | Stomach Neoplasms |
| ID | Term |
|---|---|
| D005770 | Gastrointestinal Neoplasms |
| D004067 | Digestive System Neoplasms |
| D009371 | Neoplasms by Site |
| D009369 | Neoplasms |
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| Standard anesthesia | Behavioral | Maintaining the blood pressure based on anesthesiologist's decision |
|
| D004066 |
| Digestive System Diseases |
| D005767 | Gastrointestinal Diseases |
| D013272 | Stomach Diseases |