Remifentanil use in surgery with Analgesia Nociception Index.
Conditions
Interventions
Intervention 1: Control group: Patients who are candidates for spinal surgery who undergo general anesthesia without ANI monitoring. Intervention 2: Intervention group: Patients who are candidates for
Sponsors
Tehran University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 70 Years
Inclusion criteria
Inclusion criteria: Patients between 18 and 70 years Patients candidate for spine surgery ASA Grade I-II Consent to enter the study
Exclusion criteria
Exclusion criteria: Patients taking beta-blocker drugs
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Dosage of remifentanil during surgery. Timepoint: During surgery. Method of measurement: The amount of remifentanil consumed. | — |
Secondary
| Measure | Time frame |
|---|---|
| The rate of pain in recovery in patients. Timepoint: 10, 20, 30 and 60 minutes during recovery. Method of measurement: Visual Analogue Scale.;Further drop in arterial blood saturation below 90% for 60 seconds. Timepoint: 10, 20, 30 and 60 minutes during recovery. Method of measurement: Pulse oximetry.;Complications of fentanyl remedies. Timepoint: During recovery. Method of measurement: According to the recovery nurse.;Global Satisfaction of patients at the end of recovery. Timepoint: At the end of recovery. Method of measurement: Based on 5 point criteria (poor, average, good, very good and excellent). | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactFarsad Imani
Tehran University of Medical Sciences
Outcome results
None listed