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Clinical Trial Summary

In this prospective randomized controlled trial, the subjects will be assigned to group transcutaneous electrical acupoint stimulation (TEAS) and group control (no intervention). The postoperative outcomes including NIHSS (National Institute of Health stroke scale) score, morbidity and mortality will be evaluated during hospital stay and by one year after surgery.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05413460
Study type Interventional
Source Air Force Military Medical University, China
Contact Zhihong Lu
Phone +8613891975018
Email deerlu23@163.com
Status Recruiting
Phase N/A
Start date July 26, 2022
Completion date June 30, 2023

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