None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: ?American Society of Anesthesiologists classification I, II, III ? Patients over 30 years of age and under 90 years of age who agreed to participate in the study ? Patients undergoing total knee arthroplasty (TKA) performed at our hospital
Exclusion criteria
Exclusion criteria: ? Patients with infection at the site where the blockage was performed ? Patients with chronic opiate dependence ?Patients with morbid obesity (BMI>35) ?Patients with pre-existing neurological deficits ? Patients with bleeding tendency ? Patients with hypersensitivity to Remifentanil or Ropivacaine ? Patients with uncontrolled diabetes ?Pregnant women ?Patients with psychoscocial problems ?Patient's refusal ?Patients who do not understand how to use PCA ? Patients with impaired left ventricular function due to cardiac output < 0.35
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Cumulative IV Fentanyl Consumption 48 Hours Post-operatively | — |
Secondary
| Measure | Time frame |
|---|---|
| vital sign change during operation;qNOX change during operation;hypotension during operation;bradycardia during operation;operation time;time taken for block;anesthesia time;Time of first request for opioid analgesic;Pain intensity 6 hours after operation;Pain intensity 12 hours after operation;Pain intensity 24 hours after operation;Pain intensity 48 hours after operation;Pain intensity 72 hours after operation;Cumulative IV Fentanyl Consumption 6 Hours Post-operatively;Cumulative IV Fentanyl Consumption 12 Hours Post-operatively;Cumulative IV Fentanyl Consumption 24 Hours Post-operatively;Cumulative IV Fentanyl Consumption 48 Hours Post-operatively;Cumulative IV Fentanyl Consumption 72 Hours Post-operatively;Remifentanil dose during operation;side effects after operation;blood transufusion;sleep satisfaction;Satisfaction with pain control | — |
Countries
Korea, Republic of
Contacts
Dong-A University Hospital