Displaying 1 - 10 of 28 for Heart
  • ADAPT Response (H-38200)
    • AdaptivCRT® (aCRT) algorithm CRT devices in reducing incidence of the combined endpoint of all-cause mortality and intervention for heart failure decompensation compared to standard CRT therapy
  • aMAZE Trial (H-37863)
    • The purpose of this study is to evaluate the safety and effectiveness of the LARIAT System in the treatment of subjects with symptomatic persistent or longstanding persistent atrial fibrillation.
  • Biomarker Variability and Predictive Value in Dyspnea (H-37226)
    • A study to evaluate regional differences in biomarker values and in clinical outcomes in dyspneic patients
  • Cardiovascular Study (H-30665)
    • 12-21 year old adolescents and young adults (normal weight and overweight) with and without type 2 diabetes are needed for a research study investigating risk for heart disease in youth.
  • Cheers Study: Childhood Hypertension (H-35753)
    • The purpose of this study is to evaluate the efficacy and safety of the study drug relative to an active comparator losartan which the same class of drug and is approved for use in the pediatric population aged 6 years and older.
  • Effect of Diabetes Medication on Blood Sugar Levels and Liver/Heart Fat (H-29171)
    • The purpose of this study is to investigate the effect of a diabetes medication on blood sugar levels and liver and heart fat in adults who are at high risk for developing diabetes.
  • Effect of Nutritional Supplements on Cell Function and Metabolism (H-29575)
    • The purpose of this study is to identify specific biomarkers of obesity and diabetes that cause increased risk for heart disease and diabetes in healthy and obese subjects and to test in the lab if nutritional supplements can reduce this risk.
  • Fatty Liver (H-31469)
    • This study is investigating the risk for early heart disease in youth (ages 11-21) and involves body composition, liver scan and blood tests.
  • Genetic Basis of Cardiovascular Malformations (H-32836)
    • Researchers at Baylor College of Medicine are testing a new way to find whether a piece of the genetic material is lost, duplicated, or misspelled.
  • Genetic Study of CHARGE Association (H-7697)
    • CHARGE is a genetic disorder that is caused by mutations in at least two different genes. One of the genes has been discovered. In this study we are attempting identify other genes that might cause the condition.