Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Acute Lymphoblastic Leukemia
  • Lymphoma
  • Pediatric ALL
  • Pediatric Cancer
  • Pediatric Lymphoma
Type
Interventional
Phase
Phase 1
Design
Allocation: RandomizedIntervention Model: Crossover AssignmentIntervention Model Description: The study uses a prospective randomized controlled crossover study design.Masking: None (Open Label)Primary Purpose: Supportive Care

Participation Requirements

Age
Between 1 years and 17 years
Gender
Both males and females

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 Do...

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.

Tracking Information

NCT #
NCT03964259
Collaborators
Not Provided
Investigators
Principal Investigator: Cady P Noda, PharmD Virginia Commonwealth University