The purpose of this study is to study the effects of intermittent whole-body hypoxic preconditioning on patients with carotid artery stenosis.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Enrollment
50
Patients will be treated with mild hypoxia ( Note: The oxygen concentration decreased from 20% to 18%, and keeping at 18%)×7 days,twice a day in the morning and in the afternoon before surgery.
Patients will be treated with sham preconditioning (oxygen concentration: 21%) ×7 days,twice a day in the morning and in the afternoon before surgery.
Tianjin HuanHu Hospital
Tianjin, Tianjin Municipality, China
Respiratory rate
Time frame: Before, during and 5 min after the intervention.
Heart rate
Time frame: Before, during and 5 min after the intervention.
Systolic blood pressure
Time frame: Before, during and 5 min after the intervention.
Arterial blood oxygen saturation
Time frame: Before, during and 5 min after the intervention.
Hemoglobin content
Time frame: On admission, and at the 1st day after surgery.
Hypoxia inducible factor-1α
Time frame: On admission, and at the 1st day after surgery.
Erythropoietin
Time frame: On admission, and at the 1st day after surgery.
Vascular endothelial growth factor
Time frame: On admission, and at the 1st day after surgery.
Neuron-specific enolase
Time frame: On admission, and at the 1st day after surgery.
S100β protein
Time frame: On admission, and at the 1st day after surgery.
Brain-derived neurotrophic factor
Time frame: On admission, and at the 1st day after surgery.
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Serum aspartate transaminase
Time frame: On admission, and at the 1st day after surgery.
Serum alanine aminotransferase
Time frame: On admission, and at the 1st day after surgery.
Serum creatinine
Time frame: On admission, and at the 1st day after surgery.
Blood urea nitrogen
Time frame: On admission, and at the 1st day after surgery.
The incidence of adverse events
Time frame: During the intervention.
Average length of hospital stay
Time frame: Through study completion, an average of 3 months.
Postoperative complications
Time frame: Through study completion, an average of 3 months.