Search clinical trials for: Congenital Muscular Dystrophy

Total 21723 results

Boston University

Completed

Phase II Study of Arginine Butyrate With or Without Epoetin Alfa in Patients With Thalassemia Intermedia

Beta-Thalassemia

United States, United Kingdom
Eunice Kennedy Shriver National Institute of Child...

Unknown

The Effect of 5-Alpha Reductase on Testosterone in Men

Sex Disorders

United States
Institute of Child Health

Completed

Trial of Nutritional Supplementation in Infants Born Small for Gestational Age

Birth Weight

United Kingdom
Rambam Health Care Campus
Lumenis Be Ltd.

Unknown

Evaluation and Optimization of the Technical and Clinical Performance of the Lumenis ONE Platform

Port Wine Stain | Telangiectases

Israel
iTech Medical, Inc.

Unknown

Study to Demonstrate That Muscle Pattern Recognition (MPR) is an Effective Evaluation Tool for Musculoskeletal Neck or Back Pain

Low Back Pain | Neck Pain

United States, Canada
National Taiwan University Hospital

Unknown

Establish a CT Images Database of Patients With Congenital Heart Disease

Heart Diseases

Taiwan
National Taiwan University Hospital

Unknown

Evaluating the Infant Complex Congenital Heart Disease by Multidetector Computed Tomography

Heart Diseases

Taiwan
Albert Schweitzer Hospital

Completed

Treatment of Malaria With Quinine Plus Sulfadoxine-Pyrimethamine

Malaria

Gabon
Centers for Disease Control and Prevention
Ministry of Health, Honduras; Project Healthy Children

Completed

Dosage Effects of Folic Acid on Blood Folates of Honduran Women

Spina Bifida and Anencephaly

Honduras
University of Johannesburg

Completed

Routine Versus Selective Midtrimester Ultrasound in a Poorly Resourced Setting: a Cluster Randomised Controlled Trial

Fetal Congenital Abnormalities | Prolonged Pregnancy | Multiple Pregnancy

South Africa
National Taiwan University Hospital

Unknown

Mutation Analysis of 17α-Hydroxylase

Hypertension | Congenital Adrenal Hyperplasia | Pseudohermaphroditism

Taiwan
National Taiwan University Hospital

Unknown

Aortic Regurgitation After Surgical Repair of Outlet-Type Ventricular Septal Defect

Aortic Valve Insufficiency | Heart Septal Defects, Ventricular

Taiwan
National Taiwan University Hospital

Unknown

Congenital or Idiopathic Complete Right Bundle Branch Block: Physiological Significance and Molecular Characterization

Bundle-Branch Block

Taiwan
Centers for Disease Control and Prevention

Completed

Limb Loss Self-Management Program

Congenital or Acquired Limb Deficiency

United States
Gustave Roussy, Cancer Campus, Grand Paris

Terminated

Rhabdomyosarcoma and Malignant Soft Tissue Tumours of Childhood

Rhabdomyosarcoma | Malignant Soft Tissue

France
National Taiwan University Hospital

Unknown

Quantitative Analysis of SMN1 and SMN2 Gene Based on DHPLC System

Spinal Muscular Atrophy

Taiwan
National Taiwan University Hospital

Unknown

Evaluation of Immune Function in Biliary Atresia Children With Prolonged Jaundice

Biliary Atresia

Taiwan
Makerere University
Ministry of Health, Uganda; Sanofi-Synthelabo

Unknown

Efficacy of Intrarectal Versus Intravenous Quinine for the Treatment of Childhood Cerebral Malaria

Cerebral Malaria

Uganda
Eunice Kennedy Shriver National Institute of Child...

Unknown

Evaluating the Effectiveness of a Dichloroacetate in MELAS Syndrome

MELAS Syndrome

United States
National Center for Research Resources (NCRR)
James Whitcomb Riley Hospital for Children

Completed

Phase II Pilot Study of Granulocyte Colony-Stimulating Factor for Inherited Bone Marrow Failure Syndromes

Thrombocytopenia | Dyskeratosis Congenita | Fanconi's Anemia | Shwachman Syndrome
National Institute of Neurological Disorders and...
Seattle Children's Hospital

Unknown

Phase II Randomized Study of Selective Dorsal Rhizotomy and Physiotherapy Vs Physiotherapy Alone for Spastic Diplegia

Spastic Diplegia
National Institute of Neurological Disorders and...
Baylor College of Medicine

Completed

Study of Phenotype and Genotype Correlations in Patients With Contiguous Gene Deletion Syndromes

Prader-Willi Syndrome | DiGeorge Syndrome | Williams Syndrome | Angelman Syndrome | Smith-Magenis Syndrome | Chromosome Abnormalities | Shprintzen Syndrome

United States
University of Minnesota

Unknown

Phase I Pilot Study of CD34 Enriched, Fanconi's Anemia Complementation Group C Gene Transduced Autologous Peripheral Blood Stem Cell Transplantation in Patients With Fanconi's Anemia

Fanconi's Anemia
National Center for Research Resources (NCRR)
Northwestern University

Completed

Phase II Pilot Study of Extracorporeal Phototherapy for Epidermolysis Bullosa Acquisita

Epidermolysis Bullosa Acquisita
National Center for Research Resources (NCRR)
University of California, Los Angeles

Completed

Stem Cell Transplantation (SCT) for Genetic Diseases

Thrombocytopenia | Inborn Errors of Metabolism | Metachromatic Leukodystrophy | Fanconi's Anemia | Thalassemia Major | Pure Red-Cell Aplasia

United States
National Center for Research Resources (NCRR)
Yale University

Completed

Phase III Randomized, Placebo-Controlled, Crossover Study of Soy Protein Isolate for Hereditary Hemorrhagic Telangiectasia

Hereditary Hemorrhagic Telangiectasia
Eunice Kennedy Shriver National Institute of Child...

Completed

Evaluating Muscle Function After Ankle Surgery

Muscle Weakness | Muscle Atrophy | Fractures

United States
Royal Brompton & Harefield NHS Foundation Trust
CORDA, The Heart Charity; Apotex Inc.; The Cooley's Anemia Foundation,; The UK...

Unknown

Combined Chelation Treatment With Deferiprone and Deferoxamine in Thalassemia Major

Beta-Thalassemia

Italy
National Center for Research Resources (NCRR)
National Institute of Allergy and Infectious Diseases (NIAID)

Completed

Phase III Randomized, Controlled Study of Ganciclovir for Symptomatic Congenital Cytomegalovirus Infection

Cytomegalovirus Infections
National Center for Research Resources (NCRR)
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) and other collaborators

Completed

Establishment of the National Epidermolysis Bullosa Registry

Epidermolysis Bullosa
National Center for Research Resources (NCRR)

Completed

Vitamin D Metabolism and the Williams Syndrome

Williams Syndrome

United States
National Center for Research Resources (NCRR)
Ohio State University

Completed

Phase III Randomized, Double-Blind, Placebo-Controlled Study of Dichlorphenamide for Periodic Paralyses and Associated Sodium Channel Disorders

Paralysis, Hyperkalemic Periodic | Paramyotonia Congenita | Hypokalemic Periodic Paralysis
National Center for Research Resources (NCRR)
Ann & Robert H Lurie Children's Hospital of Chicago

Completed

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

Heart Defects, Congenital | Tetralogy of Fallot | Pulmonary Valve Stenosis | Hypoparathyroidism | Pulmonary Atresia | Conotruncal Cardiac Defects
National Center for Research Resources (NCRR)
University of California, San Diego

Completed

Evaluation of Fanconi Syndrome and Cystinosis

Fanconi Syndrome | Cystinosis
National Heart, Lung, and Blood Institute (NHLBI)

Completed

Cooperative Study of The Clinical Course of Sickle Cell Disease

Anemia, Sickle Cell | Blood Disease
National Center for Research Resources (NCRR)
National Institute of Allergy and Infectious Diseases (NIAID)

Completed

Phase I/II Study of Human Anti-Cytomegalovirus (CMV) Monoclonal Antibody MSL-109 in Newborns With Symptomatic Congenital CMV Infection Without Central Nervous System Disease

Cytomegalovirus Infections
National Center for Research Resources (NCRR)

Completed

Effects of Exercise on Markers of Inflammation in Skeletal Muscle in Elderly Hip Fracture Patients

Muscular Atrophy | Hip Fractures

United States
Fairview University Medical Center

Completed

Study of Allogeneic Bone Marrow Transplantation Following Cyclophosphamide and Radiotherapy in Patients With Fanconi's Anemia

Fanconi's Anemia

United States
National Center for Research Resources (NCRR)
Baylor College of Medicine

Completed

Study of the Nutritional, Metabolic, and Body Composition Profile in Children and Adolescents With Epidermolysis Bullosa

Epidermolysis Bullosa
ZonMw: The Netherlands Organisation for Health...
Boston Scientific Corporation

Completed

Emmy Trial: Uterine Artery Embolization (UAE) Versus Hysterectomy for Uterine Fibroids

Uterine Neoplasms | Leiomyoma | Menorrhagia

Netherlands
National Center for Research Resources (NCRR)
Baylor College of Medicine

Completed

Phase II Randomized Study of Leuprolide Vs Oral Contraceptive Therapy Vs Leuprolide and Oral Contraceptive Therapy for Ovarian Hyperandrogenism

Hyperandrogenism
National Center for Research Resources (NCRR)
University of Michigan

Completed

Pilot Study of the Effect of Baclofen and Bromocriptine on Luteinizing Hormone Secretion in Pubertal Children

Growth Disorders
National Center for Research Resources (NCRR)
Yale University

Completed

Phase II Pilot Study of Octreotide, a Somatostatin Octapeptide Analog, for Gastrointestinal Hemorrhage in Hormone-Refractory Hereditary Hemorrhagic Telangiectasia and Senile Ectasia

Hereditary Hemorrhagic Telangiectasia | Ectasia
RespireRx
FRAXA Research Foundation

Completed

Effects of CX516 on Functioning in Fragile X Syndrome and Autism

Fragile X Syndrome | Autism

United States
National Center for Research Resources (NCRR)
Children's Hospital of Philadelphia

Completed

Diagnostic Pilot Study of Dual Energy Absorptiometry in the Detection of Osteopenia or Osteoporosis in Patients With Thalassemia Major

Osteoporosis | Osteopenia | Thalassemia Major
Dana-Farber Cancer Institute

Unknown

Phase I Study of Amifostine in Patients With Bone Marrow Failure Related to Fanconi's Anemia

Fanconi's Anemia

United States
National Center for Research Resources (NCRR)
Northwestern University

Completed

Study of Genotype and Phenotype Expression in Congenital Nephrogenic Diabetes Insipidus

Diabetes Insipidus, Nephrogenic
National Center for Research Resources (NCRR)
University of Vermont

Completed

Studies of Hereditary Hemorrhagic Telangiectasia

Telangiectasia, Hereditary Hemorrhagic
National Center for Research Resources (NCRR)
Shirley Ryan AbilityLab

Completed

Pilot Study of Fructose for Sickle Cell Crisis

Sickle Cell Anemia
Fairview University Medical Center

Completed

Study of Allogeneic Bone Marrow Transplantation Following Cyclophosphamide and Radiotherapy in Patients With Myelodysplastic Syndrome and Acute Leukemia Related to Fanconi's Anemia

Myelodysplastic Syndromes | Leukemia, Lymphocytic, Acute | Fanconi's Anemia | Leukemia, Nonlymphocytic, Acute

United States

Search clinical trials for: Congenital Muscular Dystrophy

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