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NCT01683448 · ClinicalTrials.gov registry record
The Effect of Perioperative Medications on the Outcomes of Patients Undergoing Cardiac Surgery
A clinical trial, sponsored by University of California, Davis.
- Completed
- Registry status
- 1
- Enrollment target
NCT01683448: Completed study, sponsored by University of California, Davis.
NCT01683448 is a clinical trial that has completed, run by University of California, Davis. The registered enrollment target is 1 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01683448 has completed, sponsored by University of California, Davis.
- COMPLETED
- Registry status
- 1 participants
- Enrollment target
Study Summary
This study will be a retrospective study. The patient data from the electronic medical records and existing database will be collected and analyzed. Primary endpoints will be postoperative mortality (within 30 days) and overall complications and length of hospital stay. The secondary endpoints will be myocardial infarction, cardiac death, CHF, arrhythmia, ischemia, stroke, neurological complications, length of ICU stay, re-admission rate, infections, pulmonary complications, length of intubation time, length of ventilation time, and acute renal failure.
Primary Outcome
blood pressure and heart rare
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 1 participants |
| Start Date | 2010-02 |
| Est. Completion | 2015-02 |
What the finished NCT01683448 record still lists
NCT01683448 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 1 participants, a relatively small participant target.
The record links to 0 conditions, and to 0 interventions.
NCT01683448 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01683448 about?
NCT01683448 is a clinical study titled "The Effect of Perioperative Medications on the Outcomes of Patients Undergoing Cardiac Surgery". This study will be a retrospective study. The patient data from the electronic medical records and existing database will be collected and analyzed. Primary endpoints will be postoperative mortality (within 30 days) and overall complications and length of hospital stay. The secondary endpoints will ...
What is the current status of trial NCT01683448?
This trial is currently completed. The enrollment target is 1 participants. The study started on 2010-02. Estimated completion is 2015-02.
Who is sponsoring clinical trial NCT01683448?
This trial is sponsored by University of California, Davis, which has 657 total clinical trials registered on ClinicalTrials.gov.
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