multiple fractures of spine, level unspecified. Fracture of spine, level unspecified
Conditions
Interventions
Intervention 1: Intervention group: patients with spinal surgery whom received Remifentanil Infusion as Remifentanil Hydrochloride I.V. 1mg, sold under the brand name EPAXIR, Exir Pharmaceutical Co. w
Sponsors
Ilam University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Patients with spinal surgery taking Remifentanil Patients with spinal surgery taking Sufentanil Patients with spinal surgery taking Methadone
Exclusion criteria
Exclusion criteria: Patients with Psychological History Patients with History of Drug Addiction Patients with History of Allergic Reaction to Drugs Patients with History of Diabetes Patients with History of Kidney Disease
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Delirium Severity and Duration. Timepoint: After Spinal Surgery, 6, 12, and 24 Hours After Surgery. Method of measurement: Physical Examination.;Four Main Delirium Features. Timepoint: After Spinal Surgery, 6, 12 and 24 Hours After Surgery. Method of measurement: CAM-ICU(Confusion Assessment Method for the Intensive Care Unit) Questionnaire.;Pain Intensity Score. Timepoint: After Spinal Surgery, 6, 12 and 24 Hours After Surgery. Method of measurement: Visual Analog Scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactHamidreza Zanji
Ilam University of Medical Sciences
Outcome results
None listed