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CompletedNCT00919438FARMUpdated Feb 4, 2010

Non Invasive External Monitoring in Dialysis Patients

An observational study in Kidney Failure, sponsored by Corventis, Inc.. Completed. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2010-02-04.

Sponsored by Corventis, Inc. · Observational

Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
25
Ages
18 Years and older
Sex
All
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Study 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.

Read the detailed description

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

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Conditions studied

  • Kidney Failure

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03

In context

Renal Insufficiency

1,995 studies on the registry are indexed under Renal Insufficiency; 173 are open to participants now.

This study's planned enrollment of 25 is below the median of 149 across 394 observational studies indexed under Renal Insufficiency.

Browse Renal Insufficiency studies →

Lead sponsor

Corventis, Inc. is the lead sponsor of 7 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Primary care and kidney failure clinics

Inclusion criteria

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

Exclusion criteria

Exclusion Criteria:

  • Is participating in another clinical study that may confound the results of this study
05

Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
25 participants (estimated)

Groups and cohorts

  • Dialysis

    Device: AVIVO™ Mobile Patient Management System

Interventions

  • DeviceAVIVO™ Mobile Patient Management System

    Non Invasive monitoring device

    Also known as: Diuretics- oral or IV

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Study locations

No study locations are listed for this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 4, 2010, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00919438
Lead sponsor
Corventis, Inc.
First posted
Jun 12, 2009
Start date
Jan 2009
Primary completion
Sep 2009
Completion
Sep 2009
Last update
Feb 4, 2010

Study contacts

Inder Anand, MD
principal investigator · VAMC, MN
Imad Libbus, PhD
study director · Corventis, Inc.

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Feb 2010. You cannot join it, but the record below documents what was studied.

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