National Institutes of Health: Genetic Diseases, Inborn trials

The registry lists 24 Genetic Diseases, Inborn studies with National Institutes of Health as lead sponsor. 8 are open to participants now and 1 have results posted.

Phase 2 1No phase 23(a study in two phases counts in both)

Studies

Open to participants first, then studies with results posted, then the rest; newest registration first within each.

• Acceptance and Commitment Therapy for Caregivers of Children With a RASopathy: An Internal Pilot Feasibility Study and Follow-up Randomized Controlled TrialRecruitingNCT05361811Not applicable
• Clinical and Genetic Evaluation of Individuals With Undiagnosed Disorders Through the Undiagnosed Diseases NetworkRecruitingNCT02450851
• Inherited Reproductive DisordersRecruitingNCT01500447
• Genome Medical Sequencing for Gene DiscoveryRecruitingNCT01087320
• Screening Protocol for Genetic Diseases of Lymphocyte Homeostasis and Programmed Cell DeathRecruitingNCT00246857
• Evaluation of Patients With Immune Function AbnormalitiesRecruitingNCT00128973
• Recruitment and Apheresis Collection of Peripheral Blood Hematopoietic Stem Cells, Mononuclear Cells and GranulocytesRecruitingNCT00001405
• Familial Mediterranean Fever and Related Disorders: Genetics and Disease CharacteristicsRecruitingNCT00001373
• Etidronate for Arterial Calcifications Due to Deficiency in CD73 (ACDC)CompletedNCT01585402Phase 2Results posted
• Pediatric Patients With Metabolic or Other Genetic DisordersCompletedNCT02769949
• Insights Into Microbiome and Environmental Contributions to Sickle Cell Disease and Leg Ulcers Study (INSIGHTS Study)CompletedNCT02156102
• Skeletal Muscle Biomarkers in People With Fragile Sarcolemmal Muscular DystrophyActive, not recruitingNCT01851447
• Studying Childhood-onset Behavioral, Psychiatric, and Developmental DisordersCompletedNCT01778504
• Brain-Derived Neurotrophic Factor in Obesity and Brain FunctionCompletedNCT01517048
• Inherited Diseases, Caregiving, and Social NetworksCompletedNCT01498263
• The Role of Family Functioning in Promoting Adaptation in Siblings of Individuals With Duchenne Muscular Dystrophy (DMD)TerminatedNCT01386515
• Next Generation to Identify Genetic Causes of Disease in Patients Participating in NICHD Clinical ProtocolsCompletedNCT01375543
• Personalized Genomic ResearchCompletedNCT01294345
• Screening Protocol for Genetic Diseases of Allergic InflammationCompletedNCT00852943
• Genetic Studies in the Amish and MennonitesCompletedNCT00359580
• Genetic Studies of X-linked Lymphoproliferative DiseaseCompletedNCT00359411
• Studies of Children With Metabolic and Other Genetic DisordersCompletedNCT00025870
• Microarray Analysis for Human Genetic DiseaseCompletedNCT00001898
• Study of Clinical and Molecular Manifestations of Genetic DisordersCompletedNCT00001466