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Genetic Diseases, Inborn

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Genetic Diseases, Inborn

Explore clinical trials studying Genetic Diseases, Inborn. Study availability and eligibility vary by location and protocol.

12,578 public trials 2,158 recruiting studies

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Genetic Diseases, Inborn trial results

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Clinical Validation of AI-Based Quantitative Eye Movement Analysis From Smartphone 9-Gaze Videos (Glandy EOM)

NCT07623837

Conditions: Autoimmune Diseases, Central Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +24 more
Locations: 3003 North First Street #221 San Jose, California, United States

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Exploring Lived Experiences of Families of Children With Spinal Muscular Atrophy(SMA) Type 1 Regarding Feeding and Communication

NCT07596277

Conditions: Behavior, Central Nervous System Diseases, Communication, +20 more
Locations: GSTT Evelina Neurosciences London, United Kingdom

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Validity and Reliability of the International Physical Fitness Questionnaire and the Self-Perceived Health-Related Physical Fitness Questionnaire in Children and Adolescents With JIA and FMF

NCT07617558

Conditions: Arthritis, Arthritis, Juvenile, Autoimmune Diseases, +11 more
Locations: Not specified

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Adjunctive Oral Iron Supplementation in Atopic Dermatitis

NCT07613190

Conditions: Atopic Dermatitis, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dermatitis, +13 more
Locations: Not specified

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Probiotic-Uricase Complex Preparation for Improving Uric Acid Metabolism in Patients With Hyperuricemia

NCT07613164

Conditions: Arthritis, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Crystal Arthropathies, +13 more
Locations: Not specified

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High-Dose Vitamin C in G6PDA and Pyruvate Kinase Deficiency: A Safety Study

NCT07612345

Conditions: Anemia, Anemia, Hemolytic, Anemia, Hemolytic, Congenital, +12 more
Locations: University of Utah Salt Lake City, Utah, United States

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Phase III Clinical Trial of Changji'an Capsules in the Treatment of Irritable Bowel Syndrome With Predominant Diarrhea (Liver-Qi Invading Spleen Syndrome)

NCT07610434

Conditions: Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, +9 more
Locations: Beijing Hospital of Traditional Chinese Medicine Beijing, Dongcheng District, China

West China Hospital, Sichuan University Chengdu, China

Chongqing Traditional Chinese Medicine Hospital Chongqing, China

The First Affiliated Hospital of Guangzhou University of Chinese Medicine Guangzhou, China

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Preventive Dendritic Cell Vaccination for Lynch Syndrome Carriers

NCT07609901

Conditions: Colonic Diseases, Colorectal Neoplasms, Colorectal Neoplasms, Hereditary Nonpolyposis, +15 more
Locations: Radboudumc Nijmegen, Gelderland, Netherlands

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Treatment Patterns, Biochemical Profiles and Clinical Outcomes in Adults With X-Linked Hypophosphatemia

NCT07607600

Conditions: Avitaminosis, Bone Diseases, Bone Diseases, Metabolic, +26 more
Locations: Yale University School of Medicine New Haven, Connecticut, United States

Indiana University Hospital Indianapolis, Indiana, United States

The Ohio State University Wexner Medical Center (OSUWMC) - CarePoint East Columbus, Ohio, United States

Vanderbilt University Medical Center Nashville, Tennessee, United States

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Denys-Drash Syndrome and Risk of Post-transplant Lymphoproliferative Disorder

NCT07605884

Conditions: Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Denys-Drash Syndrome, +21 more
Locations: Hôpital Femme Mère Enfant, Hospices Civils de Lyon Bron, France

CHU de Lille Lille, France

CHU Montpellier Montpellier, France

CHU de Nancy - Hôpitaux de Brabois Nancy, France

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Genetic Diseases, Inborn

Genetic Diseases, Inborn trial results

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