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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.

449 public trials 107 recruiting studies

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Genetic Diseases, Inborn trial results

Completed

Newborn Genomic Sequencing Pilot Study

NCT06276348

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Disease, Genetic Diseases, Inborn
Locations: Rady Children's Hospital San Diego San Diego, California, United States

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Completed

Intra-Erythrocyte Dexamethasone Sodium Phosphate in Ataxia Teleangiectasia Patients

NCT01255358

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Genetic Syndrome, +2 more
Locations: Spedali Civili Brescia, Italy

University La Sapienza Rome, Italy

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Completed

Prospective, Non-interventional Study to Evaluate the Effectiveness of Elocta Compared to Conventional Factor Products

NCT02976753

Conditions: Blood Coagulation Disorders, Blood Coagulation Disorders, Inherited, Coagulation Protein Disorders, +6 more
Locations: Swedish Orphan Biovitrum Research site Innsbruck, Austria

Swedish Orphan Biovitrum Research site Linz, Austria

Swedish Orphan Biovitrum Research Site Sankt Pölten, Austria

Swedish Orphan Biovitrum Research site Vienna, Austria

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Completed

A Study to Evaluate the Real-world Usage and Effectiveness of Elocta and Alprolix in Patients With Haemophilia A or B

NCT03055611

Conditions: Blood Coagulation Disorders, Blood Coagulation Disorders, Inherited, Coagulation Protein Disorders, +10 more
Locations: Swedish Orphan Biovitrum Reserach site Berlin, Germany

Swedish Orphan Biovitrum Reserach Site Blaubeuren Abbey, Germany

Swedish Orphan Biovitrum Research Site Bonn, Germany

Swedish Orphan Biovitrum Research Site Delmenhorst, Germany

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Completed

HEMAGO Monitoring and Impact on the Occurrence of Complications During Pregnancy in Sickle Cell Patients

NCT06620887

Conditions: Anemia, Anemia, Hemolytic, Anemia, Hemolytic, Congenital, +7 more
Locations: Service de gynécologie-obstétrique de l'Hôpital Femme Mère Enfant Bron, France

Croix-Rousse Hospital - Service de Gynécologie-Obstétrique Lyon, France

Service de gynécologie-obstétrique de l'Hôpital de Lyon Sud Lyon, France

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Completed

A Study to Evaluate the Real-world Effectiveness and Usage of Alprolix in Patients With Haemophilia B in France

NCT03655340

Conditions: Blood Coagulation Disorders, Blood Coagulation Disorders, Inherited, Coagulation Protein Disorders, +8 more
Locations: Swedish Orphan Biovitrum Research Site (CHU de Bordeaux) Bordeaux, France

Swedish Orphan Biovitrum Research Site Brest, France

Swedish Orphan Biovitrum Research Site Caen, France

Swedish Orphan Biovitrum Research Site Chambéry, France

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Completed

Genetic Screening and Assisted Oocyte Activation in Couples with Diminished/aberrant Embryonic Development.

NCT03354013

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Embryo, Embryo Disorder, +2 more
Locations: Ghent University Hospital Ghent, East-Flandres, Belgium

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Completed

Guanfacine Extended Release for the Reduction of Aggression and Self-injurious Behavior Associated With Prader-Willi Syndrome

NCT05657860

Conditions: Aberrant Motor Behavior in Dementia, Abnormalities, Multiple, Aggression, +34 more
Locations: Maimonides Medical Center Brooklyn, New York, United States

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Completed

Genetic Study of the Dilatations of the Idiopathic Bronchi in French Polynesia

NCT04417777

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Idiopathic Bronchiectasis
Locations: CH Polynesie Française Papeete, French Polynesia

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Completed

A Comprehensive Approach To Relief Of Digestive Symptoms In Cystic Fibrosis: CARDS-CF

NCT05251467

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cystic Fibrosis, Digestive System Disease, +8 more
Locations: Nottingham University Hospitals NHS Trust Nottingham, United Kingdom

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Genetic Diseases, Inborn

Genetic Diseases, Inborn trial results

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