Clinical Trials Logo
  1. Home
  2. Spinal Diseases
  3. NCT06123624
  4. Details
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)
See also
  Status Clinical Trial Phase
Recruiting NCT05484557 - Prevention of Thromboembolism Using Apixaban vs Enoxaparin Following Spinal Cord Injury N/A
Not yet recruiting NCT02535273 - The Effect of Dexmedetomidine Analgesia and Sedation in Minimally Invasive Spine Surgery Under Local Anesthesia Phase 4
Recruiting NCT02187653 - Intraoperative Monitoring (IOM) Patient Registry N/A
Completed NCT00295009 - Safety and Effectiveness Study of Prodisc to Spinal Fusion Surgery N/A
Completed NCT03832036 - The Diagnostic and Prognostic Value of Two Quantitative Clinical Tests in Patients With Lumbar Disc Herniation N/A
Completed NCT03015142 - Observational Clinical Study to Plan, Position and Check Instrument Placement for Spine Surgery Interventions
Completed NCT03158766 - Subclinical Propionibacterium Acnes Infection Estimation in the Intervertebral Disc (SPInE-ID)
Not yet recruiting NCT02416557 - Effect of PEEP on Intraoperative Hypothermia N/A
Completed NCT02724111 - Effect of Neuromuscular Blockade on Operating Conditions and Overall Satisfaction During Spinal Surgery Phase 4
Enrolling by invitation NCT03492372 - Molecular Characterization of Spinal Tissue
Completed NCT03753945 - Spine MRI in Patients With Deep Brain Stimulation (DBS) N/A
Terminated NCT03802656 - Vertebral Body Tethering Treatment for Idiopathic Scoliosis N/A
Recruiting NCT02809781 - A Pilot Study of MSCs Iufusion and Etanercept to Treat Ankylosing Spondylitis Phase 2/Phase 3
Not yet recruiting NCT02762656 - The Effect of Perioperative Lidocaine Intravenous Infusion on Postoperative Recovery After Spine Surgery. Phase 4
Completed NCT00808665 - Intraoperative Infusion of Precedex to Reduce Length of Stay After Lumbar Spine Fusion Phase 4
Completed NCT00756301 - Cutaneous Administration of Local Anesthetic for Spine Injection Procedures N/A
Completed NCT03562455 - Virtual Reality for Power Wheelchair Training N/A
Completed NCT00942227 - The Value of Traction in Treatment of Lumbar Radiculopathy Phase 3
Completed NCT01020929 - Incidence of Simultaneous Epidural and Intravascular Injection N/A
Completed NCT00979108 - The Value of Traction in the Treatment of Cervical Radiculopathy Phase 3