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NCT01103908 · ClinicalTrials.gov registry record
Cardiac Output Measurement at the Conclusion of Cardiopulmonary Bypass
A clinical trial, sponsored by Transonic Systems.
- Terminated
- Registry status
- 3
- Enrollment target
NCT01103908 is a clinical trial that was terminated before completion, run by Transonic Systems. The registered enrollment target is 3 participants.
The verdict
NCT01103908 was terminated before completion, sponsored by Transonic Systems.
- TERMINATED
- Registry status
- 3 participants
- Enrollment target
Study Summary
Cardiac output, the amount of blood pumped by the heart in one minute, will be measured in pediatric patients undergoing surgery involving cardiopulmonary bypass (CPB). Cardiac output will be measured after cardiopulmonary bypass using a device that employs ultrasound dilution technology. At times, cardiac output will be measured during a procedure called modified ultrafiltration (MUF). The ultrasound dilution cardiac output measurements will be validated or compared with cardiac output measurements made using other FDA approved techniques and devices.
Interventions
- DEVICE HCE101 Cardiopulmonary Support Monitor
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 3 participants |
| Start Date | 2010-04 |
| Est. Completion | 2011-08 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01103908
The ClinicalTrials.gov registry entry for NCT01103908 describes a study currently listed as terminated, categorized as an unspecified phase. The registered enrollment target is 3 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Transonic Systems, which has 12 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which HCE101 Cardiopulmonary Support Monitor is the first listed.
NCT01103908 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01103908 about?
NCT01103908 is a clinical study titled "Cardiac Output Measurement at the Conclusion of Cardiopulmonary Bypass". Cardiac output, the amount of blood pumped by the heart in one minute, will be measured in pediatric patients undergoing surgery involving cardiopulmonary bypass (CPB). Cardiac output will be measured after cardiopulmonary bypass using a device that employs ultrasound dilution technology. At times, ...
What is the current status of trial NCT01103908?
This trial is currently terminated. The enrollment target is 3 participants. The study started on 2010-04. Estimated completion is 2011-08.
What interventions are being tested in trial NCT01103908?
The interventions under investigation include: HCE101 Cardiopulmonary Support Monitor (DEVICE).
Who is sponsoring clinical trial NCT01103908?
This trial is sponsored by Transonic Systems, which has 12 total clinical trials registered on ClinicalTrials.gov.
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