None
Conditions
Interventions
Experimental group:The infusion fluid is heated to 39 centigrade, Anesthesia full depth monitor
Control Group:Anesthesia full depth monitor
Sponsors
Beijing Chest Hospital, Capital Medical University
Eligibility
Sex/Gender
All
Age
30 Years to 60 Years
Inclusion criteria
Inclusion criteria: ? Lung cancer patients aged 130-60(including those aged 30 and 60) ? Informed consent was received from patients who agreed to participate in the study
Exclusion criteria
Exclusion criteria: ? Patients allergic to propofol ? Previous neurological impairment of the related limbs ? Those with mental illness who can not cooperate
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain index;Pain scores; | — |
Secondary
| Measure | Time frame |
|---|---|
| Hemodynamics; | — |
Countries
China
Contacts
Public ContactLiu Tao
Department of Anesthesiology, Beijing Chest Hospital, Capital Medical University
Outcome results
None listed