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Clinical Trial Summary

To determine whether a reduced volume hydration regimen will lead to a shorter time to methotrexate clearance when compared to a standard intravenous (IV) hydration regimen.


Clinical Trial Description

This study uses a prospective randomized controlled crossover study design. Neither patients nor clinicians are blinded to the standard versus reduced intravenous fluids (IVF) regimen. Patients are randomized to begin with standard volume or reduced volume IVF. Over the course of 4 cycles of High Dose Methotrexate (HDMTX), patients alternate between standard and reduced volume post hydration fluids protocols. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03964259
Study type Interventional
Source Virginia Commonwealth University
Contact
Status Completed
Phase Phase 1
Start date October 2, 2019
Completion date December 28, 2022

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