Factors Associated With Hyponatremia Induced by High-dose Cyclophosphamide

Status Not yet recruiting

Clinical Trial Summary

Prospoctive cohort of high-dose cyclophosphamide exposed patients. With active estandardize screening of hyponatremia development in the follow up period.

Clinical Trial Description

Primary objectives

1. To identify the factors associated with the development of hyponatremia in patients receiving high-dose cyclophosphamide (2.5 grams or more).

2. Generate and validate a predictive score of developing hyponatremia high-dose cyclophosphamide.

3. To estimate the incidence of hyponatremia in patients undergoing high-dose cyclophosphamide.

Study design. Observational prospective cohort study of Patients after infusion of high-dose cyclophosphamide. Follow up period will be from cyclophosphamide infusion until one month after hospital discharge. ;

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Hyponatremia

Clinical Trial Details

NCT number	NCT02399358
Study type	Observational
Source	Hospital Italiano de Buenos Aires
Contact	Fernando Warley, MD
Phone	+54 9 11 61541958
Email	fernando.warley@hospitalitaliano.org.ar
Status	Not yet recruiting
Phase	N/A
Start date	December 2015
Completion date	November 2017

View Details

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