Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
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: Clinical Trial study, sponsored by Transonic Systems.
NCT01103908 is a clinical trial that was terminated before completion, run by Transonic Systems. The registered enrollment target is 3 participants. According to ClinicalTrials.gov, the official US trial registry.
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.
Primary Outcome
Cardiac output will be measured in pediatric patients after undergoing surgery involving cardiopulmonary bypass
Interventions
- DEVICE HCE101 Cardiopulmonary Support Monitor
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 3 participants |
| Start Date | 2010-04 |
| Est. Completion | 2011-08 |
Why NCT01103908 stopped before completion
NCT01103908 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 3 participants, a relatively small participant target.
The record links to 0 conditions, and to 1 intervention - of which HCE101 Cardiopulmonary Support Monitor is the first listed.
NCT01103908 does not publish any study locations in the registry export this page uses.
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.
Learn More About Clinical Trials
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar registry start date
- NCT05988463 · started 2027-01-01 · Phase 1
Dose-Escalation Study of Artesunate Patients With IPF
- NCT07219706 · started 2026-12-10 · NA
Dietary Fiber and Time Restricted Eating
- NCT02831335 · started 2026-12-01
Technical Development of Multi-Parametric Renocerebral MRI
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia