Cardiac Diseases Clinical Trial
Official title:
The Use of Colloid Versus Crystalloid in Post-operative Pediatric Cardiac Patients for Fluid Resuscitation
Verified date | March 2017 |
Source | Vanderbilt University Medical Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of the study is to help determine if either crystalloid solution or colloid solution is more advantageous as a resuscitative fluid in post-operative pediatric cardiac patients.
Status | Completed |
Enrollment | 32 |
Est. completion date | July 2009 |
Est. primary completion date | July 2009 |
Accepts healthy volunteers | No |
Gender | All |
Age group | N/A to 36 Months |
Eligibility |
Inclusion Criteria: - Congenital heart defect with two ventricle anatomy and physiology - Ages: 0 - 36 months of age Exclusion Criteria: - History of bleeding disorder - History of renal disorder |
Country | Name | City | State |
---|---|---|---|
United States | The Monroe Carell, Jr. Children's Hospital at Vanderbilt | Nashville | Tennessee |
Lead Sponsor | Collaborator |
---|---|
Vanderbilt University Medical Center |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | maintenance of hemodynamic stability according to an age specific, predetermined, minimal mean arterial blood pressure | Throughout the post operative period | ||
Secondary | lactate clearance | Throughout the post operative period | ||
Secondary | inotropic requirements | throughout the post operative period | ||
Secondary | establishment of adequate urine output | Throughout the post operative period | ||
Secondary | post-operative occurrence of edema (peripheral and pulmonary) | Througout the post operative period | ||
Secondary | monitoring of cost difference as determined by total number of boluses, number of ventilator hours, and length of ICU stay | Throughout the ICU stay |
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