Status:
COMPLETED
Different Anesthesia Maintain Protocol Effect the Outcome of the Patients
Lead Sponsor:
China International Neuroscience Institution
Conditions:
Urinary Surgery
General Anesthesia
Eligibility:
All Genders
18-65 years
Phase:
PHASE4
Brief Summary
This prospective open-label randomized study, patients were having elective urological surgery scheduled to last longer than 1 h under necessitating general anesthesia.Group-P: (Propofol group): 3 mg ...
Detailed Description
Group-P: (Propofol group): 3 mg kg-1 min-1 propofol was pumped continuously after endotracheal intubation. Group-PAS: (Propofol and after 20 min adding Sevoflurane group): 3 mg kg-1 min-1 propofol wer...
Eligibility Criteria
Inclusion
- the aged 18-65 yr,
- ASA physical status I, II or III patients
- having elective urological surgery
- operation scheduled to last longer than 1 h
- under necessitating general anesthesia
Exclusion
- refused to participate in the study;
- were not able to communicate due to alterations in the level of consciousness, - a history of allergy to opioids
- contraindications inhalational anaesthesia
- family history of malignant hyperthermia
- alcohol or drug abuse
- received central nervous system-active drugs;
- body mass index ≥40 kg/m2
- represent conditions liable to alter the pharmacokinetic and pharmacodynamic behaviors of the intravenous and inhalation anesthetics
- previous head injury, neurologic or psychiatric disease
- any disabling central nervous
- cerebrovascular disease
- current use of psychoactive or anti-convulsive medications
- unstable angina
- manifest congestive heart failure
- airway management was expected to be difficult
Key Trial Info
Start Date :
June 25 2020
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
August 5 2020
Estimated Enrollment :
50 Patients enrolled
Trial Details
Trial ID
NCT04443946
Start Date
June 25 2020
End Date
August 5 2020
Last Update
October 14 2020
Active Locations (1)
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1
Xuanwu hospital
Beijing, Beijing Municipality, China, 100053