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The primary purpose of this study is to compare the desflurane and sevoflurane on remifentanil requirement using analgesia nociception index-guided anesthesia in patients undergoing spine surgery.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Desflurane group | Experimental |
| |
| Sevoflurane group | Placebo Comparator |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Desflurane Inhalation Solution | Drug | Keeping the anesthesia using desflurane inhalation solution as 1 minimal alveolar concentration |
|
| 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 3 hours) |
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Inclusion Criteria:
Exclusion Criteria:
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| ID | Term |
|---|---|
| D013122 | Spinal Diseases |
| ID | Term |
|---|---|
| D001847 | Bone Diseases |
| D009140 | Musculoskeletal Diseases |
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| Sevoflurane Inhalation Solution | Drug | Keeping the anesthesia using sevoflurane inhalation solution as 1 minimal alveolar concentration |
|