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Clinical Trial Summary

To evaluate the safety of Fosaprepitant Dimeglumine Injection for the prevention of nausea and vomiting caused by tumor chemotherapy drugs, analyze the characteristics of the applicable population and clinical medication of Fosaprepitant Dimeglumine, evaluate the risk factors that may affect the efficacy of drug use, and compare the clinical benefits of different drug use modes.


Clinical Trial Description

This is a prospective, one arm, open, non-interference, multi center, observational, real world clinical study. Study drug: Fosaprepitant Dimeglumine for injection. White or almost white lump or powder, containing 150mg (calculated as C23H22F7N4O6P). This product is a NK-1 receptor antagonist, which is administered jointly with other antiemetic drugs. It is suitable for adult patients to prevent acute and delayed nausea and vomiting during the initial and repeated treatment of highly emetic chemotherapy drugs (HEC). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05755659
Study type Interventional
Source Xijing Hospital
Contact Hong Liu
Phone 0086-13709284513
Email hongliu1@fmmu.edu.cn
Status Recruiting
Phase N/A
Start date July 15, 2022
Completion date December 20, 2024

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