KCT0006904
Recruiting
未知
Comparison of requirements for deep neuromuscular block effect during continuous and intermittent bolus injection of rocuronium in patients under general anesthesia: a randomized equivalence trial
ConditionsNot Applicable
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not Applicable
- Sponsor
- Kosin University Gospel Hospital
- Enrollment
- 62
- Status
- Recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\) Patients aged 18\-65 years
- •2\) Patients undergoing general anesthesia for elective abdominal (gastrointestinal tract, colon and rectal, liver) surgery
- •3\) Patients whose operation time is expected to be more than 2 hours
- •3\) Patients corresponding to American Society of Anesthesiologist Status 1\-2
Exclusion Criteria
- •1\) Patients under total venous anesthesia
- •2\) Emergency surgery patients
- •3\) body mass index \= 30 kg/m2
- •4\) Pregnant and lactating women
- •5\) Patients with lung diseases such as asthma and COPD
- •6\) Patients with a history of treatment for cerebrovascular disease
- •7\) Patients allergic to drugs (including neuromuscular blocking agent):
- •\- Patients with a history of hypersensitivity to sevoflurane, desflurane, or other halogenated anesthetics.
- •\- Patients with a history of hypersensitivity to remifentanil and other fentanyl analogues all.
- •\- Patients with a history of hypersensitivity to rocuronium and any of its components or neuromuscular blockers
Outcomes
Primary Outcomes
Not specified
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