Zero Sodium Peritoneal Dialysate Protocol Pilot Study

Status Completed

Clinical Trial Summary

The following pilot study will be undertaken to determine the effects of use of a zero-sodium peritoneal dialysate solution (10% dextrose in sterile water) on sodium removal as compared to a standard peritoneal dialysis solution.

Clinical Trial Description

While heart failure (HF) is generally regarded as the inability of the heart to pump sufficient blood, on a population level, volume overload is the primary driver of morbidity and hospitalization. The signs and symptoms of volume overload are driven by water accumulation, which is initially driven by sodium retention. This overall goal of this study is to investigate the ability to remove sodium through use of a zero-sodium solution in peritoneal dialysis. ;

Study Design

Related Conditions & MeSH terms

Heart Failure
Potential Applications for Heart Failure
Volume Overload

Clinical Trial Details

NCT number	NCT03801226
Study type	Interventional
Source	Yale University
Contact
Status	Completed
Phase	Early Phase 1
Start date	December 1, 2018
Completion date	May 31, 2019

View Details

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