Postoperative Fatigue Syndrome
Conditions
Interventions
Control group:none
Sponsors
The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1. Living kidney donors 2. ASA Level I or II 3. Age 18-65 years old 4. BMI 18~28kg/m2
Exclusion criteria
Exclusion criteria: 1. Severe Neuropsychiatric Disorders 2. Coagulation dysfunction and skin infection at the puncture site 3. Glaucoma and thyroid enlargement 4. Recent history of myocardial infarction and abnormal cardiac excitatory conduction 5. Communication barriers 6. History of stellate ganglion block
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| the Christensen score and ICFS score ; | — |
Secondary
| Measure | Time frame |
|---|---|
| Level of serum tumor necrosis factor (TNF)-a, interleukin (IL)-6, S100ß protein, C-reactive protein and neuron-specific enolase (NSE). ;creatinine;Urine output;VAS;the dosage of both propofol and remifentanil;Douleur Neuropathique 4 questions,DN4;operative time;PONV;hospital stay; | — |
Countries
China
Contacts
Public ContactJuan Li
The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China
Outcome results
None listed