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NCT06123624 Clinical Trial

Desflurane and Sevoflurane on Remifentanil Requirement

Spinal Diseases Clinical Trial

Official title:
Comparison of Desflurane and Sevoflurane on Remifentanil Requirement Using Analgesia Nociception Index-guided Anesthesia

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT06123624
Other study ID # AJOUIRB-IV-2023-380
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date November 27, 2023
Est. completion date August 30, 2024

Study information
Verified date November 2023
Source Ajou University School of Medicine
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 78
Est. completion date August 30, 2024
Est. primary completion date August 30, 2024
Accepts healthy volunteers No
Gender All
Age group 19 Years to 80 Years
Eligibility Inclusion Criteria: - Clinical diagnosis of herniated disc, injury of spinal cord, and neoplasm of spinal meninges Exclusion Criteria: - Hyperbilirubinemia - Prior chronic pain - Prior opioid abuse - Cardiac arrythmia

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• Desflurane Inhalation Solution
Keeping the anesthesia using desflurane inhalation solution as 1 minimal alveolar concentration
• Sevoflurane Inhalation Solution
Keeping the anesthesia using sevoflurane inhalation solution as 1 minimal alveolar concentration

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Ajou University School of Medicine

Outcome
Type Measure Description Time frame Safety issue
Primary 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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