Non Invasive External Monitoring in Dialysis Patients

NCT ID: NCT00919438

Last Updated: 2010-02-04

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

25 participants

Study Classification

OBSERVATIONAL

Study Start Date

2009-01-31

Study Completion Date

2009-09-30

Brief Summary

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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

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

Conditions

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Kidney Failure

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Study Groups

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Dialysis

AVIVO™ Mobile Patient Management System

Intervention Type DEVICE

Non Invasive monitoring device

Interventions

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AVIVO™ Mobile Patient Management System

Non Invasive monitoring device

Intervention Type DEVICE

Other Intervention Names

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Diuretics- oral or IV

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Corventis, Inc.

INDUSTRY

Sponsor Role lead

Responsible Party

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Corventis

Principal Investigators

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Inder Anand, MD

Role: PRINCIPAL_INVESTIGATOR

VAMC, MN

Imad Libbus, PhD

Role: STUDY_DIRECTOR

Corventis, Inc.

Other Identifiers

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COR-2008-001

Identifier Type: -

Identifier Source: org_study_id

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