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Clinical Trial Summary

According to the inclusion and exclusion criteria, a total of 108 patients were enrolled and randomly divided into control group (n = 56) and intervention group (n = 52). The control group received routine nursing, while the intervention group received upper limb lymphedema prevention program for breast cancer patients after surgery. Before surgery, at the third chemotherapy (about 2.1 months after surgery) and the sixth chemotherapy (about 4.2 months after surgery), the self-designed general information questionnaire was used to investigate the patient's basic situation, and the corresponding tools were used to measure the volume of the patient's upper arm, the grip strength of the affected arm, and the range of motion of the affected shoulder joint.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05595330
Study type Interventional
Source First Affiliated Hospital Xi'an Jiaotong University
Contact
Status Completed
Phase N/A
Start date March 1, 2020
Completion date December 8, 2020

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