Adult elective lung surgery patients undergoing general anesthesia and thoracic epidural anesthesia
Conditions
Interventions
0.2% ropivacaine 10ml grou
0.375% ropivacaine 10ml group
0.75% ropivacaine 10ml group
Sponsors
Department of Anesthesiology, Niigata University Medical and Dental Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Adult elective lung surgery patients undergoing general anesthesia and thoracic epidural anesthesia
Exclusion criteria
Exclusion criteria: 1)Neuromuscular diseases 2)Remarkable neurological symptoms 3)Contraindications for epidural anesthesia 4)History of Allergy to ropivacaine or drugs on the protocol 5)Estimated the trial entry inappropriate
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Percent changes in the amplitude of motor evoked potentials in a lower extremity at 60 minutes after the epidural ropivacaine administration. | — |
Secondary
| Measure | Time frame |
|---|---|
| 1)Percent changes in the amplitudes of motor evoked potentials in lower extremities at 15, 30, 45, 90, 120, 150 and 180 minutes after the epidural ropivacaine administration. 2)Percent changes in the amplitudes of somatosensory evoked potentials in lower extremities after the epidural ropivacaine administration. 3)Percent changes in the latency of motor evoked potentials in lower extremities after the epidural ropivacaine administration. 4)Percent changes in the latency of somatosensory evoked potentials in lower extremities after the epidural ropivacaine administration. | — |
Countries
Japan
Contacts
Public ContactToshiyuki Tobita
Niigata University Medical and Dental Hospital Department of Anesthesiology
Outcome results
None listed