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TerminatedNCT00920569Updated May 27, 2016

Recirculation, Oxygenator Blood Volume and Cardiac Output Measurements During Extracorporeal Membrane Oxygenation

An observational study in Recirculation, Oxygenator Blood Volume and Cardiac Output, sponsored by Transonic Systems Inc.. Terminated at 1 site in United States. Per ClinicalTrials.gov, last updated 2016-05-27.

Sponsored by Transonic Systems Inc. · Observational

Why this study was terminated
Study site collaborators withdrew from participating due to time constraints.
Study type
Observational
Time perspective
Prospective
Enrollment
8
Sex
All
01

Study summary

This study is to test the usefulness of ultrasound dilution measurements in patients on extracorporeal membrane oxygenation. Measurements may include; efficiency of support (recirculation), amount of clotting in the oxygenator (oxygenator blood volume), and how well the heart is working (cardiac output). At the present time there are no devices available to perform these functions.

Read the detailed description

At the present time there are no devices available to measure recirculation, oxygenator blood volume and cardiac output in patients on extracorporeal membrane oxygenation. The study uses an external monitor, laptop computer, clamp on flowsensors and ultrasound dilution technology to measure blood flow. Measurements are made by injecting 0.5 - 1 ml/kg of sterile isotonic saline into the patient's extracorporeal circuit. The subject will be monitored throughout the measurements. The measurements will be coordinated with the regular care of the extracorporeal circuit.

02

Conditions studied

  • Recirculation
  • Oxygenator Blood Volume
  • Cardiac Output
  • Venoarterial Extracorporeal Membrane Oxygenation
  • Venovenous Extracorporeal Membrane Oxygenation

Keywords

  • cardiac output
  • recirculation
  • oxygenator blood volume
  • venoarterial extracorporeal membrane oxygenation
  • venovenous extracorporeal membrane oxygenation
03

In context

Lead sponsor

Transonic Systems Inc. is the lead sponsor of 17 studies on the registry; none are open to participants now.

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

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Measurement of cardiac output in venoarterial extracorporeal membrane oxygenation patients, recirculation in venovenous extracorporeal membrane oxygenation patients and oxygenator blood volume in venoarterial and venovenous extracorporeal membrane oxygenation patients.

Inclusion criteria

  • Neonatal, pediatric or adult patients receiving venoarterial or venovenous extracorporeal membrane oxygenation.

Exclusion criteria

Exclusion Criteria:

  • Patients not receiving venoarterial or venovenous extracorporeal membrane oxygenation.
05

Study design

Time perspective
Prospective
Enrollment
8 participants (actual)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Cardiac output, recirculation or oxygenator blood volume measurements made in patients receiving extracorporeal membrane oxygenation.

    Time frame: Duration of extracorporeal membrane oxygenation

07

Study locations

1 site
  • University of Michigan, Medical School
    Ann Arbor, Michigan 48109, United States
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 27, 2016, 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
NCT00920569
Lead sponsor
Transonic Systems Inc.
Collaborators
National Heart, Lung, and Blood Institute (NHLBI)
Responsible party
Sponsor
First posted
Jun 15, 2009
Start date
May 2006
Primary completion
Aug 2008
Completion
Aug 2008
Last update
May 27, 2016

Study contacts

Jonathan Haft, MD
principal investigator · University of Michigan
Nikolai M Krivitski, PhD, DSc
principal investigator · Transonic Systems Inc.

Oversight

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

Not currently enrolling

This study is terminated, as verified in May 2016. You cannot join it, but the record below documents what was studied.

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