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Clinical Trial Summary

The aim of this study is to investigate the effects of remote ischaemic preconditioning on the peripheral blood characteristics of healthy adults and to explore the possible mechanisms for improving ischaemia/reperfusion injury and its protective effects on the cardiovascular system.


Clinical Trial Description

This study will recruit 40 healthy individuals and randomly assign them to group A or B to undergo remote ischaemic preconditioning training for 7 consecutive days, and routine biological specimens from subjects before and after the intervention will be collected. Participants in group A will be trained once a day, while those in group be will be trained twice a day. The characteristics of different fractions of blood and urine and fecal specimens from subjects at different time points before and after ischaemic preconditioning will be examined to investigate the effects of remote ischaemic preconditioning on the characteristics of peripheral blood, urine and feces in healthy adults. It also provides evidence for improving the efficiency of clinical transfusion and blood conservation by comparing the differences in blood fractions under different preservation conditions. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05957523
Study type Interventional
Source First Affiliated Hospital Xi'an Jiaotong University
Contact Guoliang Li
Phone 0086-029-13759982523
Email liguoliang_med@163.com
Status Not yet recruiting
Phase N/A
Start date May 20, 2024
Completion date December 12, 2024

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