Non Invasive External Monitoring in Dialysis Patients

Completed

• Conditions: Kidney Failure
• Interventions: Device: AVIVO™ Mobile Patient Management System

• Registration Number: NCT00919438
• Lead Sponsor: Corventis, Inc.

Brief Summary

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.

Detailed Description

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

Study Timeline

• Study Start: 2009-01
• Study First Submitted: 2009-06-10
• Study First Submitted QC: 2009-06-11
• Study First Posted: 2009-06-12
• Primary Completion: 2009-09
• Study Completion: 2009-09
• Status Verified: 2010-02
• Last Update Submitted: 2010-02-02
• Last Update Posted: 2010-02-04

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 25

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

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
Dialysis	AVIVO™ Mobile Patient Management System	-