Non Invasive External Monitoring in Dialysis Patients

This is a single center, non randomized study to gather data to correlate physiological signals with the patient's fluid status during fluid removal in hemodialysis.

Completed

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Key information

Conditions

Kidney Failure Female Urogenital Diseases Female Urogenital Diseases and Pregnancy Complications Kidney Diseases Male Urogenital Diseases Renal Insufficiency Urogenital Diseases Urologic Diseases

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

About this study

Patients undergoing hemodialysis will be monitored with the study device . The collected information will be correlated with fluid loss.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Is female or male, 18 years of age or older
Undergoing hemodialysis for fluid removal

Exclusion criteria

Is participating in another clinical study that may confound the results of this study

Treatment and study plan

AVIVO™ Mobile Patient Management System

Device

Non Invasive monitoring device

Other names: Diuretics- oral or IV

Sponsors and collaborators

Lead sponsor

Corventis, Inc.

Industry

Registry information

Official study title

Fluid Removal During Adherent Renal Monitoring

Acronym: FARM

Important dates

Study start: 2009
Primary completion: 2009
Study completion: 2009
First posted: Jun 12, 2009
Registry last updated: Feb 4, 2010

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed