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Heart Defects, Congenital clinical trials

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NCT ID: NCT00005153 Completed - Clinical trials for Cardiovascular Diseases

Etiologic Risk Factors of Cardiovascular Malformations

Start date: December 1980
Phase: N/A
Study type: Observational

To identify genetic and environmental risk factors for congenital cardiac disease.

NCT ID: NCT00004828 Completed - Clinical trials for Heart Defects, Congenital

Liothyronine in Children With Single Ventricle Congenital Cardiac Malformations Undergoing the Fontan Procedure

Start date: December 1994
Phase: Phase 1
Study type: Interventional

OBJECTIVES: I. Determine the pharmacokinetics of exogenous liothyronine administered in children undergoing the modified Fontan procedure. II. Determine the liothyronine supplementation dose that counters the fall in serum liothyronine concentrations and provides the greatest potential myocardial benefit after the modified Fontan procedure. III. Evaluate the potential toxicity of exogenous liothyronine administered in children undergoing a modified Fontan procedure.

NCT ID: NCT00004361 Completed - Clinical trials for Heart Defects, Congenital

Study of the Relationship Between Calcium Levels and Intact Parathyroid Hormone (iPTH) in Adults With Repaired or Palliated Conotruncal Cardiac Defects

Start date: July 1995
Phase: N/A
Study type: Observational

OBJECTIVES: I. Identify latent hypoparathyroidism in normocalcemic adult survivors with repaired conotruncal cardiac defects, by evaluating parathyroid gland secretory function after induced hypocalcemia. II. Determine the relationship of parathyroid hormone secretion to microdeletions in the same region of chromosome 22q11 as found in patients with DiGeorge anomaly.

NCT ID: NCT00001460 Completed - Arrhythmia Clinical Trials

Evaluation and Treatment of Heart Disease in Patients Not Participating in Research

Start date: January 1995
Phase: N/A
Study type: Interventional

There is an important need to maintain clinical skills, provide quality training and expertise, and provide an environment that stimulates ideas for clinical research. This study permits inpatient evaluation and management of patients with heart disease who do not qualify to participate in studies currently being conducted by the Cardiology Branch of the National Heart, Lung, and Blood Institute.

NCT ID: NCT00000494 Completed - Clinical trials for Cardiovascular Diseases

Management of Patent Ductus in Premature Infants

Start date: September 1978
Phase: Phase 3
Study type: Interventional

To evaluate the effects (up to one year of age) of indomethacin on the clinical course of patent ductus arteriosus (PDA) in premature infants (24 hours old or less) and to assess the relative merits of indomethacin and surgery in infants with persistent respiratory distress who were not treated early with indomethacin. Two concurrent trials were performed.

NCT ID: NCT00000470 Completed - Clinical trials for Cardiovascular Diseases

Infant Heart Surgery: Central Nervous System Sequelae of Circulatory Arrest

BCAS
Start date: December 1988
Phase: Phase 3
Study type: Interventional

To compare the influence of two surgical anesthetic techniques, hypothermia with circulatory arrest or hypothermia with low-flow bypass perfusion, on neurologic functioning in infants undergoing heart surgery.

NCT ID: NCT00000107 Completed - Clinical trials for Heart Defects, Congenital

Body Water Content in Cyanotic Congenital Heart Disease

Start date: n/a
Phase: N/A
Study type: Observational

Adults with cyanotic congenital heart disease have elevated levels of plasma proatrial natruretic peptide (proANP) which most likely results in chronic dehydration, leading to reduced oxygen transport to tissues and shortness of breath with activity. The purpose of this study is to characterize adults with cyanotic congenital heart defects with respect to their body composition (water and fat-free mass) and resting metabolic rates. The study consists of several measures of how much body water, fat and lean tissue a subject has, and measures the number of calories the subject's body uses at rest. Adult subjects with cyanotic congenital heart disease will be recruited along with healthy noncyanotic control subjects matched for age, gender, and body weight.