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NCT01103895 · ClinicalTrials.gov registry record
Measurement of Cardiac Output Before and After Cardiopulmonary Bypass.
A clinical trial, sponsored by Transonic Systems.
- Terminated
- Registry status
- 14
- Enrollment target
NCT01103895: Clinical Trial study, sponsored by Transonic Systems.
NCT01103895 is a clinical trial that was terminated before completion, run by Transonic Systems. The registered enrollment target is 14 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01103895 was terminated before completion, sponsored by Transonic Systems.
- TERMINATED
- Registry status
- 14 participants
- Enrollment target
Study Summary
Cardiac output, the amount of blood pumped by the heart in one minute, will be measured in adults undergoing surgery involving cardiopulmonary bypass. Cardiac output will be measured before and after cardiopulmonary bypass using a device that employs ultrasound dilution technology. The ultrasound dilution cardiac output measurements will be validated or compared with cardiac output measurements made using thermodilution, which is the current "gold standard."
Primary Outcome
Cardiac output will be measured using an ultrasound dilution technique and compared with cardiac output measured using thermodilution after the completion of surgical procedures involving cardiopulmonary bypass.
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 14 participants |
| Start Date | 2007-07 |
| Est. Completion | 2012-05 |
Why NCT01103895 stopped before completion
NCT01103895 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 14 participants, a relatively small participant target.
The record links to 0 conditions, and to 0 interventions.
NCT01103895 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01103895 about?
NCT01103895 is a clinical study titled "Measurement of Cardiac Output Before and After Cardiopulmonary Bypass.". Cardiac output, the amount of blood pumped by the heart in one minute, will be measured in adults undergoing surgery involving cardiopulmonary bypass. Cardiac output will be measured before and after cardiopulmonary bypass using a device that employs ultrasound dilution technology. The ultrasound di...
What is the current status of trial NCT01103895?
This trial is currently terminated. The enrollment target is 14 participants. The study started on 2007-07. Estimated completion is 2012-05.
Who is sponsoring clinical trial NCT01103895?
This trial is sponsored by Transonic Systems, which has 12 total clinical trials registered on ClinicalTrials.gov.
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