Clinical Trials on Genetic Blood Group (bg) Polymorphism in U Negativity and St(a) of MNSs

Total 7 results

  • Blood Donation Service Zurich, SRC
    Unknown
    Whole Genome Sequencing for Blood Group Genotyping and Definition as Exemplified on U- and St(a)+. (Blood Genome)
    Genetic Blood Group (bg) Polymorphism in U Negativity and St(a) of MNSs
    Switzerland
  • National Taiwan University Hospital
    Completed
    Efficacy Study of Telbivudine in Chronic Hepatitis B Patients
    Chronic Hepatitis B | Roadmap Concept in Chronic Hepatitis B Treatment | 24-week PCR Negativity of Telbivudine | PCR Negativity at 52 and 104 Week | HBeAg Seroconversion Rate at 52 and 104 Week
    Taiwan
  • Hamad Medical Corporation
    Unknown
    Effect of Taurine on Glycemic Control in Type I and Type II Diabetic Patients
    it is a Group of Metabolic Diseases in | Which a Person Has High Blood Sugar, Either | Because the Body Does Not Produce Enough Insulin, | or Because Cells do Not Respond to the Insulin That | is Produced.
  • Anagnostou, Evdokia, M.D.
    The Hospital for Sick Children; Canadian Institutes of Health Research (CIHR); Alberta Health services and other collaborators
    Not yet recruiting
    Sertraline vs. Placebo in the Treatment of Anxiety in Children and AdoLescents With NeurodevelopMental Disorders (CALM)
    Anxiety Disorders | Generalized Anxiety Disorder | Anxiety | Tuberous Sclerosis | ADHD | Neurodevelopmental Disorders | Autism Spectrum Disorder | Fragile X Syndrome | Social Anxiety | Social Anxiety Disorder | Agoraphobia | Tourette Syndrome | Tic Disorders | Autism | ADHD Predominantly Inattentive Type | ADHD - Combined... and other conditions
    Canada
  • Assistance Publique - Hôpitaux de Paris
    Not yet recruiting
    Development of Non-Invasive Prenatal Diagnosis for Single Gene Disorders (DANNIgene)
    Hemophilia A | Hemophilia B | Cystic Fibrosis | Sickle Cell Disease | Muscular Dystrophy, Duchenne | Fragile X Syndrome | Huntington Disease | Myotonic Dystrophy | Autosomal Recessive Polycystic Kidney Disease | Neurofibromatosis-Noonan Syndrome | Muscular Dystrophy, Becker | Invasive PreNatal Diagnosis in a... and other conditions
    France
  • RTI International
    Eunice Kennedy Shriver National Institute of Child Health and Human Development... and other collaborators
    Enrolling by invitation
    Early Check: Expanded Screening in Newborns
    Primary Hyperoxaluria Type 3 | Diabetes Mellitus | Hemophilia A | Hemophilia B | Hereditary Fructose Intolerance | Cystic Fibrosis | Factor VII Deficiency | Phenylketonurias | Sickle Cell Disease | Dravet Syndrome | Duchenne Muscular Dystrophy | Prader-Willi Syndrome | Fragile X Syndrome | Chronic Granulomatous Disease and other conditions
    United States
  • Centre Hospitalier Universitaire de Liege
    Sanofi; Takeda; University of Liege; Orchard Therapeutics; Centre Hospitalier Régional... and other collaborators
    Recruiting
    Baby Detect : Genomic Newborn Screening
    Congenital Adrenal Hyperplasia | Hemophilia A | Hemophilia B | Mucopolysaccharidosis I | Mucopolysaccharidosis II | Cystic Fibrosis | Alpha 1-Antitrypsin Deficiency | Sickle Cell Disease | Fanconi Anemia | Chronic Granulomatous Disease | Wilson Disease | Severe Congenital Neutropenia | Ornithine Transcarbamylase... and other conditions
    Belgium

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