Central Venous Saturation (ScvO2) Monitoring in Pediatric Patients Undergoing Cardiac Surgery
Recruitment status was Recruiting
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Purpose
Children (ages 0-12) that have heart surgery are often at a high risk of developing complications and have to be continuously monitored. Part of the routine care at UCLA includes using a monitor (continuous central venous oxygen saturation-ScvO2) to measure the amount of oxygen saturation in the tissues (indirectly) during surgery and in the intensive care unit. However, there is not much data on the use and effectiveness of this monitor in comparison to other monitors used for children.
The purpose of this study is to further evaluate the effectiveness of the continuous central venous oxygen saturation (ScvO2) monitor in children and compare it with other monitors during a heart surgery. This is an observational study and the patients will not undergo any research specific procedures in the operating room (OR). The investigators will observe and record de-identified information, such as vital signs (heart rate, blood pressure, etc.), to evaluate the importance of the monitor. This study will also look at the demographics (age, gender, diagnosis, etc.) and treatments (type of surgery) received children undergoing heart surgery to improve quality of care. The investigators will also observe the same parameters in the ICU. The investigators hypothesized that low central venous saturations are associated with worse clinical outcomes.
| Condition |
|---|
|
Congenital Heart Defects Cardiac Surgery |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Prospective |
| Official Title: | Central Venous Saturation (ScvO2) Monitoring in Pediatric Patients Undergoing Cardiac Surgery |
Eligibility| Ages Eligible for Study: | up to 12 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Probability Sample |
Patients scheduled for cardiac surgery
Inclusion Criteria:
- Pediatric patients (age 0-12 years) scheduled for cardiac surgery and requiring placement of a central venous catheter.
Exclusion Criteria:
- Patients with contraindications for placement of a central venous catheter will be excluded from this study.
Contacts and Locations| Contact: Jennifer Corniea, MA | 310-206-4484 | jcorniea@mednet.ucla.edu |
| Contact: Aman Mahajan, MD, PhD | 310-267-8680 | amahajan@mednet.ucla.edu |
| United States, California | |
| UCLA | Recruiting |
| Los Angeles, California, United States, 90095 | |
| Contact: Jennifer Corniea, MA 310-206-4484 jcorniea@mednet.ucla.edu | |
More Information
No publications provided
| Responsible Party: | Aman Mahajan, MD, PhD / Principal Investigator, UCLA |
| ClinicalTrials.gov Identifier: | NCT00883922 History of Changes |
| Other Study ID Numbers: | 06-12-078-03 |
| Study First Received: | April 17, 2009 |
| Last Updated: | April 17, 2009 |
| Health Authority: | United States: Institutional Review Board |
Additional relevant MeSH terms:
|
Heart Defects, Congenital Cardiovascular Abnormalities Cardiovascular Diseases Heart Diseases Congenital Abnormalities |
ClinicalTrials.gov processed this record on June 18, 2013