This study is a prospective, randomized, single-center trial, designed to observe the effect of remote limb ischemic preconditioning on ischemic cerebral vascular disease.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Enrollment
196
The detail of RIPC included five cycles of bilateral upper limbs 5/5 min. of ischemia and reperfusion alternation. Limb ischemia was induced by inflating tourniquets to 200 mmHg. This process was placed on both arms every day.
Xuanwu Hospital, Capital Medical University
Xicheng District, Beijing P.R., China
Blood Pressure and Heart Rates;
Time frame: at the time points of baseline and 1, 15 and 30 days after BLIPC treatment
Plasma Biomarkers of Coagulation and Fibrinolysis
blood samples were collected one hour after every times of BLIPC procedure ended, and assayed with the immuno-turbidimetry assay on the coagulation laboratory autoanalyzer
Time frame: the time points of baseline and 1, 15 and 30 days after BLIPC treatment
Number of Patients Who Got New Brain Lesions
We compared the number of patients who got new lesions in the Diffusion-weighted magnetic resonance imaging (DWI-MRI)
Time frame: 300 days after treatment
The Time Point Until the First Stroke Recurrence,
These patients underwent MRI/DWI at the time of first recurrence; patients without symptoms recurrence underwent follow-up MRI/DWI at 300 days.
Time frame: At the 300-day after the initial treatment
Brain Perfusion Improvement Are Evaluated With SPECT and TCD
Brain perfusion status were evalvated by SPECT SPECT scanning was performed using a dual headed rotating gamma camera at 30 minutes after intravenous 99mTc-ECD (25mCi) bolus injection and at 40 minutes after 18F -FDG bolus injection.
Time frame: 300-day after treatment
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