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NCT01188590 · ClinicalTrials.gov registry record
Transcutaneous Carbon Dioxide Monitoring Post Cardiac Surgery: Incidence and Severity Resp Insufficiency
A clinical trial, sponsored by Baylor Research Institute.
- Completed
- Registry status
- 50
- Enrollment target
NCT01188590: Completed study, sponsored by Baylor Research Institute.
NCT01188590 is a clinical trial that has completed, run by Baylor Research Institute. The registered enrollment target is 50 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01188590 has completed, sponsored by Baylor Research Institute.
- COMPLETED
- Registry status
- 50 participants
- Enrollment target
Study Summary
The purpose for the investigators study is to investigate the severity and incidence of respiratory insufficiency using transcutaneous carbon dioxide (TcPCO2) monitoring as an adjunct to the current standard of care for early detection of inadequate ventilation in post-operative surgical in-patients undergoing cardiac surgery after discharge from intensive care unit (ICU) or post anesthesia recovery unit (PACU).
Interventions
- DEVICE TOSCA 500 monitor
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2009-11 |
| Est. Completion | 2010-01 |
What the finished NCT01188590 record still lists
NCT01188590 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 50 participants, a relatively small participant target.
The record links to 0 conditions, and to 1 intervention - of which TOSCA 500 monitor is the first listed.
NCT01188590 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01188590 about?
NCT01188590 is a clinical study titled "Transcutaneous Carbon Dioxide Monitoring Post Cardiac Surgery: Incidence and Severity Resp Insufficiency". The purpose for the investigators study is to investigate the severity and incidence of respiratory insufficiency using transcutaneous carbon dioxide (TcPCO2) monitoring as an adjunct to the current standard of care for early detection of inadequate ventilation in post-operative surgical in-patients...
What is the current status of trial NCT01188590?
This trial is currently completed. The enrollment target is 50 participants. The study started on 2009-11. Estimated completion is 2010-01.
What interventions are being tested in trial NCT01188590?
The interventions under investigation include: TOSCA 500 monitor (DEVICE).
Who is sponsoring clinical trial NCT01188590?
This trial is sponsored by Baylor Research Institute, which has 180 total clinical trials registered on ClinicalTrials.gov.
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