Home
Conditions
Genetic Diseases, Inborn

Clinical trial condition

Genetic Diseases, Inborn

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

12,656 public trials 2,147 recruiting studies

Refine in advanced search Browse all conditions

Genetic Diseases, Inborn trial results

Completed

Vitamin D as a Nutritional Neoadjuvant During Photodynamic Therapy of Basal Cell Carcinoma

NCT03467789

Conditions: Abnormalities, Multiple, Basal Cell Carcinoma, Basal Cell Nevus Syndrome, +19 more
Locations: Medical Dermatology Specialists Phoenix Phoenix, Arizona, United States

Cleveland Clinic Taussig Cancer institute, Case Comprehensive Cancer Center Cleveland, Ohio, United States

View Trial Details

Completed

Effect of Dapagliflozin on Cardiac Structure, Function and Secondary Mitral Regurgitation in Patients with Left Ventricle Dysfunction

NCT05849766

Conditions: Cardiomegaly, Cardiomyopathies, Cardiomyopathy, Dilated, +6 more
Locations: Beni-suef University Banī Suwayf, Egypt

View Trial Details

Completed

Genetics and Heart Health After Cancer Therapy

NCT03510689

Conditions: Adnexal Diseases, Breast Cancer, Breast Diseases, +25 more
Locations: Abramson Cancer Center of the University of Pennsylvania Philadelphia, Pennsylvania, United States

View Trial Details

Completed

Trial to Describe the Safety, Tolerability, and Immunogenicity of Trumenba When Administered to Immunocompromised Participants ≥10 Years of Age

NCT04893811

Conditions: Anemia, Anemia, Hemolytic, Anemia, Hemolytic, Congenital, +11 more
Locations: Fakultni Nemocnice Brno - Detska Nemocnice - Klinika Detskych Infekcnich Nemoci Center 3 Brno, Czechia

Fakultni Nemocnice Brno - Detska Nemocnice - Klinika Detskych Infekcnich Nemoci Center 3 Brno, Czechia

Fakultni nemocnice v Motole Prague, Czechia

IN-VIVO Sp. z o.o. Bydgoszcz, Poland

View all 14 locations

View Trial Details

Completed

Molecular Aspects of Preimplantation Genetic Diagnosis for NF1

NCT05149469

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +14 more
Locations: Service Laboratoire de Diagnostic Génétique - Hôpitaux Universitaires de Strasbourg Strasbourg, France

View Trial Details

Completed

Multicenter Study of Patient-reported Gastrointestinal Symptoms in People With Cystic Fibrosis

NCT03801993

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Constipation, Cystic Fibrosis, +9 more
Locations: Stanford University Medical Center Palo Alto, California, United States

Central Connecticut Cystic Fibrosis Center Hartford, Connecticut, United States

Children's National Medical Center Washington D.C., District of Columbia, United States

Nemours Children's Clinic - Pensacola Pensacola, Florida, United States

View all 26 locations

View Trial Details

Completed

Study to Evaluate QR-110 in Leber's Congenital Amaurosis (LCA) Due to the c.2991+1655A>G Mutation (p.Cys998X) in the CEP290 Gene

NCT03140969

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cranial Nerve Diseases, Eye Diseases, +14 more
Locations: University of Iowa Iowa City, Iowa, United States

Scheie Eye Institute, University of Pennsylvania Philadelphia, Pennsylvania, United States

Ghent University Hospital and Ghent University Ghent, Belgium

View Trial Details

Completed

Skin Responses and T Cell Immunology After House Dust Mite Exposure in Sensitized Atopic Dermatitis Patients

NCT05019209

Conditions: Atopic Dermatitis, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dermatitis, +18 more
Locations: Fraunhofer Institute for Toxicology and Experimental Medicine Hanover, Lower Saxony, Germany

Hannover Medical School, Department of Dermatology and Allergy Hanover, Lower Saxony, Germany

View Trial Details

Completed

Object Finder for a Retinal Prosthesis

NCT04319809

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Eye Diseases, Hereditary, +5 more
Locations: Johns Hopkins Hospital Baltimore, Maryland, United States

View Trial Details

Completed

Prospective Intervention Study on Vitamin D in Patients With Cystic Fibrosis

NCT01321905

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cystic Fibrosis, Digestive System Diseases, +5 more
Locations: Stockholm Cystic Fibrosis Center, Karolinska University Hospital Huddinge Stockholm, Sweden

View Trial Details

Genetic Diseases, Inborn

Genetic Diseases, Inborn trial results

Related conditions