Non Invasive External Monitoring in Dialysis Patients

Kidney Failure Clinical Trial

— FARM  

Official title:

Fluid Removal During Adherent Renal Monitoring

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00919438
• Other study ID #: COR-2008-001
• Status: Completed
• Phase: N/A
• First received: June 10, 2009
• Last updated: February 2, 2010
• Start date: January 2009
• Est. completion date: September 2009

Study information

• Verified date: February 2010
• Source: Corventis, Inc.
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Observational

Clinical Trial 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.

Description:

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

Recruitment information / eligibility

• Status: Completed
• Enrollment: 25
• Est. completion date: September 2009
• Est. primary completion date: September 2009
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

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

Observational Model: Case-Only, Time Perspective: Prospective

Related Conditions & MeSH terms

• Kidney Failure
• Renal Insufficiency

Intervention

Device:
• AVIVO™ Mobile Patient Management System
Non Invasive monitoring device

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Corventis, Inc.