Cyanotic Congenital Heart Disease Clinical Trial
Official title:
Probiotics in Infants With Cyanotic Congenital Heart Disease
Infants with congenital heart disease have more frequent infections and exposures to antibiotics than healthy infants. It is unknown how congenital heart disease affects the development of bacterial colonization of the intestines. It is also unknown whether probiotics will change the bacteria in the intestine of infants with heart disease to become more like those of healthy infants without heart disease. This pilot trial is designed to address these two questions.
Infants with cyanotic congenital heart disease will be randomly assigned to receive either a placebo or probiotic Bifidobacterium infantis. Comparisons will be made between the infants receiving the placebo and healthy infants without heart disease and between the infants receiving the placebo and those receiving the probiotic. ;
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor)
Status | Clinical Trial | Phase | |
---|---|---|---|
Terminated |
NCT02564796 -
Erythropoietin to Prevent Unnecessary Transfusions In Patients With Cyanotic CHD - A Prospective Control Trial
|
Phase 2 | |
Completed |
NCT05800691 -
Predicting Factors for Mortality in Congenital Heart Disease Patients After Shunt Procedure in Developing Country.
|
||
Recruiting |
NCT04891081 -
Plasma Metanephrines in Patients With Cyanotic and Acyanotic Congenital Heart Disease
|
||
Completed |
NCT02712606 -
Accuracy of Pulse Oximeter With Hypoxemic Measurements
|
||
Completed |
NCT01426542 -
Preventing Brain Injury in Infants With Congenital Heart Disease
|
Phase 1 | |
Completed |
NCT03678909 -
Cardiac Biomarkers in Patients With Single Ventricle Physiology
|
||
Completed |
NCT04125550 -
Propofol vs Sevoflurane in Cyanotic Congenital Heart Disease
|
Phase 4 |