Clinical Trials Sponsored by Evandro Chagas Institute of Clinical Research

Total 1188 results

National Human Genome Research Institute (NHGRI)

Completed

Genetic Analysis of Craniofrontonasal Syndrome

Craniofrontonasal Syndrome | CFNS

United States
National Human Genome Research Institute (NHGRI)

Completed

Immunogenetics of Visceral Leishmaniasis

Visceral Leishmaniasis

Brazil
National Human Genome Research Institute (NHGRI)

Completed

Clinical and Genetic Studies of Familial Presenile Dementia With Neuronal Inclusion Bodies

Familial Dementia With Neuroserpin Inclusion Bodies | Nervous System Heredodegenerative Disorder

United States
National Human Genome Research Institute (NHGRI)

Completed

Study of Megakaryocytes From Patients With Abnormal Platelet Vesicles

Blood Coagulation Disorders

United States
National Human Genome Research Institute (NHGRI)

Completed

Interventions to Educate An Underserved Population About Inherited Disease Risks

Healthy Volunteers

United States
National Human Genome Research Institute (NHGRI)

Completed

Psychosocial Aspects of Genetic Testing for Hereditary Nonpolyposis Colon Cancer

HNPCC | Hereditary Nonpolyposis Colon Cancer

United States
National Human Genome Research Institute (NHGRI)

Completed

Clinical Integration of Genetic Risk Assessment in Family Medicine

Genomics

United States
National Human Genome Research Institute (NHGRI)

Completed

Experiences of Genetics Patients With Visible Abnormalities Who Facilitate Teaching in Genetics Clinics

Learning

United States
National Human Genome Research Institute (NHGRI)

Completed

Developing Newborn Screening for Infants With Primary Immunodeficiency

Immune System Diseases

United States
National Human Genome Research Institute (NHGRI)

Completed

Use of Virtual Reality to Communicate Concepts of Genomics to the General Public

Healthy | Communication | Learning

United States
National Human Genome Research Institute (NHGRI)

Completed

The Experience of Uncertainty in Parents of Children With an Undiagnosed Medical Condition

Multiple Abnormalities

United States
National Human Genome Research Institute (NHGRI)

Completed

Genetic Counselors' Experiences of Moral Value Conflicts With Clients

Genetic Counseling | Moral Value Conflicts | Moral Distress

United States
National Human Genome Research Institute (NHGRI)

Completed

Gene Transfer Therapy for Severe Combined Immunodeficieny Disease (SCID) Due to Adenosine Deaminase (ADA) Deficiency: A Natural History Study

Severe Combined Immunodeficiency

United States
National Human Genome Research Institute (NHGRI)

Completed

Pilot Study of the Process of Prenatal Genetic Counseling

Genetic Counseling

United States
National Human Genome Research Institute (NHGRI)

Completed

Study of the Experiences and Needs of Parents Continuing a Pregnancy Following a Prenatal Diagnosis of Holopresencephaly

Holoprosencephaly

United States
National Human Genome Research Institute (NHGRI)

Completed

Genetic Analysis of Familial Brain Aneurysms

Intracranial Aneurysm

United States
National Human Genome Research Institute (NHGRI)

Completed

The Value of Genetic Information to Adult Adopted Individuals

Genetic Counseling | Adoption

United States
National Human Genome Research Institute (NHGRI)

Completed

Genetic Analysis of Fraser Syndrome and Fryns Syndrome

Abnormalities, Multiple | Fraser Syndrome | Fryns Syndrome | Chromosomal Abnormalities

United States
National Human Genome Research Institute (NHGRI)

Recruiting

A Natural History Study Seeks to Understand the Clinical, Genomic, Pharmacological, Laboratory, and Dietary Determinates of Pyrimidine and Purine Metabolism Disorders

Metabolic Disease | Purine-Pyrimidine Metabolism | AICDA, OMIM *605257, Immunodeficiency With Hyper-IgM, Type 2; HIGM2 | UNG, OMIM *191525, Hyper-IgM Syndrome 5 | NT5C3A<TAB>, OMIM *606224, Anemia, Hemolytic, Due to UMPH1 Deficiency | UMPS, OMIM *613891, Orotic Aciduria | DHODH, OMIM *126064,... and other conditions

United States
National Human Genome Research Institute (NHGRI)

Recruiting

Study of Skeletal Disorders

Skeletal Disorders

United States
National Human Genome Research Institute (NHGRI)

Recruiting

MK-7075 (Miransertib) in Proteus Syndrome

Proteus Syndrome

United States
National Human Genome Research Institute (NHGRI)

Recruiting

New Technology and Child Health

Healthy Volunteers

United States
National Human Genome Research Institute (NHGRI)

Recruiting

The NIH MINI Study: Metabolism, Infection, and Immunity in Inborn Errors of Metabolism

Mitochondrial Disorders | Leigh Disease | Oxidative Phosphorylation Deficiencies | Electron Transport Chain Disorders, Mitochondrial

United States
National Human Genome Research Institute (NHGRI)

Recruiting

Analysis of Specimens From Individuals With Pulmonary Fibrosis

Pulmonary Fibrosis | Healthy Volunteers | Hermansky-Pudlak Syndrome (HPS)

United States
National Human Genome Research Institute (NHGRI)

Recruiting

Study of Chediak-Higashi Syndrome

Chediak-Higashi Syndrome

United States
National Human Genome Research Institute (NHGRI)

Active, not recruiting

Genomics, Environmental Factors and Social Determinants of Cardiovascular Disease in African Americans Study (GENE-FORECAST): Sodium Intervention Trial (SIT)

Cardiovascular Disease

United States
National Human Genome Research Institute (NHGRI)

Completed

Genomics, Environmental Factors and Social Determinants of Cardiovascular Disease in African-Americans Study (GENE-FORECAST): Prospective COVID-19 Natural History Study

Heart Disease

United States
National Human Genome Research Institute (NHGRI)

Active, not recruiting

ClinSeq: A Large-Scale Medical Sequencing Clinical Research Pilot Study

Healthy Volunteers | Atherosclerotic Heart Disease

United States
National Human Genome Research Institute (NHGRI)

Completed

Where Culture Meets Genetics: Exploring Latinas Causal Attributions of Breast and Colon Cancer and Models of Disease Inheritance

Breast Cancer | Colon Cancer

United States
National Human Genome Research Institute (NHGRI)

Completed

Patient Provider Communication and Interaction in a Virtual Clinical Setting

Healthy Volunteer

United States
National Human Genome Research Institute (NHGRI)

Completed

New Approaches for Empowering Studies of Asthma in Populations of African Descent

Asthma

United States
National Human Genome Research Institute (NHGRI)

Enrolling by invitation

Genetics of Obesity, Diabetes, and Heart Disease in African Diaspora Populations

Cardiovascular Disease | Diabetes

United States
National Human Genome Research Institute (NHGRI)

Completed

A Study of the Genetic Analysis of Brain Disorders

Holoprosencephaly

United States
National Human Genome Research Institute (NHGRI)

Completed

Genetics of Type 2 Diabetes Among Han Chinese

Hypertension | Diabetes

China
National Human Genome Research Institute (NHGRI)

Completed

Personalized Genomic Research

Genetics | Birth Defects | Genetic Disease | Genetic Linkage | Genetic Variation

United States
National Human Genome Research Institute (NHGRI)

Completed

Mapping Genes for Type 2 (Non-Insulin Dependent) Diabetes Mellitus

Diabetes | Genetic Variation

Norway, Finland
National Human Genome Research Institute (NHGRI)

Completed

Family Myopia Study

Myopia

United States
National Human Genome Research Institute (NHGRI)

Completed

The Genetic Basis of Acquired Heart Disease in Africa

Acquired Heart Disease | Rheumatic Heart Disease | Rheumatic Fever | Endomyocardial Fibrosis

Uganda, Nigeria
National Human Genome Research Institute (NHGRI)

Completed

Analysis of Data From the Women's Contraceptive and Reproductive Experiences (CARE) Study

Breast Cancer

United States
National Human Genome Research Institute (NHGRI)

Completed

The Experience of Caregivers of Children With Down Syndrome

Down Syndrome

United States
National Human Genome Research Institute (NHGRI)

Completed

Adaptation and Quality of Life Among Adults With Neurofibromatosis Type I

Neurofibromatosis Type 1 | NF1 | Von Recklinghausen Disease

United States
National Human Genome Research Institute (NHGRI)

Completed

Treatment Strategies for Children With Smith-Magenis Syndrome

Mental Retardation | Sleep Disorders, Circadian Rhythm | Developmental Delay Disorders | Chromosome Deletion | Self Injurious Behavior

United States
National Human Genome Research Institute (NHGRI)

Completed

Gene Transfer Therapy for Severe Combined Immunodeficieny Disease (SCID) Due to Adenosine Deaminase (ADA) Deficiency

Severe Combined Immunodeficiency Syndrome

United States
National Human Genome Research Institute (NHGRI)

Completed

Positive Exposure: A Photography and Video Intervention for Individuals With Craniofacial Differences

Craniofacial Differences

United States
National Human Genome Research Institute (NHGRI)

Terminated

The Role of Family Functioning in Promoting Adaptation in Siblings of Individuals With Duchenne Muscular Dystrophy (DMD)

Communication | Genetic Disease

United States
National Human Genome Research Institute (NHGRI)

Terminated

Genetic Analysis of Neural Tube and Orofacial Cleft Defects in the Irish Population

Hereditary Oral Clefts | Neural Tube Defects (NTDs) | Facial Cleft Defect

United States
National Human Genome Research Institute (NHGRI)

Terminated

Genetics and Clinical Characteristics of Bardet-Biedl Syndrome

Bardet-Biedl Syndrome

United States
National Human Genome Research Institute (NHGRI)

Completed

The Role of Social Comparisons in Coping and Quality of Life Following a Prostate Cancer Diagnosis

Prostate Cancer

United States
National Human Genome Research Institute (NHGRI)

Completed

Use of Population Descriptors in Human Genetic Research

Disease | Qualitative Research | Population Groups | Genetics, Medical | Ethnology

United States
National Human Genome Research Institute (NHGRI)

Completed

Informed Consent for Whole Genome Sequencing: Ideals and Norms Referenced by Early Participants

Coronary Artery Disease | Proteus Syndrome | Familial Isolated Hyperparathyroidism | Coffin - Sins Syndrome | Dubouitz Syndrome

United States

Clinical Trials Sponsored by Evandro Chagas Institute of Clinical Research

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