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Clinical Trials on Docosahexaenoic Acid
Total 1211 results
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Cycle Pharmaceuticals Ltd.ParexelCompletedHereditary Tyrosinemia, Type ISouth Africa
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Swedish Orphan BiovitrumCompletedEfficacy and Safety of Once Daily Dosing Compared to Twice Daily Dosing of Nitisinone in HT-1 (HT-1)Hereditary Tyrosinemia, Type IBelgium, Denmark, France, Germany, Sweden
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Medical University of ViennaCompletedAcidosis, Renal Tubular
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Cytonet GmbH & Co. KGCompletedUrea Cycle DisordersGermany
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Foregut Research FoundationRecruitingHiatal Hernia Large | Gastro Esophageal Reflux | Hiatal Hernia | Hiatal Hernia, Paraesophageal | Reflux, Gastroesophageal | Reflux AcidUnited States
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Yassin Abdelghaffar Charity Center for Liver Disease...Society of Friends of Liver Patients in the Arab World (SLPAW)RecruitingHereditary Tyrosinemia, Type IEgypt
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Children's National Research InstituteBoston Children's HospitalRecruitingUrea Cycle DisordersUnited States
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Vitaflo International, LtdCompleted
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Jahra HospitalCompletedDiabetic KetoacidosisKuwait
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University of Missouri-ColumbiaCompleted
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University Hospital, ToursCompletedPhenylketonuriaFrance
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IRCCS Azienda Ospedaliero-Universitaria di BolognaUniversity of BolognaCompletedInflammation | Mortality | HyperhomocysteinemiaItaly
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Nutrition Institute, SloveniaNational Institute of Public Health, Slovenia; University Medical Centre LjubljanaCompletedThyroid Diseases | Iron-deficiency | Vitamin D Deficiency | Nutritional Status | Vitamin B 12 Deficiency | Folic Acid Deficiency | Diet | Nutrient Deficiency | Micronutrient DeficiencySlovenia
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University of JenaJena University HospitalCompletedAmyotrophic Lateral Sclerosis | Dietary Habits | Disorder of Fatty Acid MetabolismGermany
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National Institute of Neurological Disorders and...CompletedSuccinic Semialdehyde Dehydrogenase Deficiency | SSADH DeficiencyUnited States
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Cycle Pharmaceuticals Ltd.ParexelCompletedHereditary Tyrosinemia, Type ISouth Africa
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University of ZurichCompletedPhenylketonuria (PKU) and HyperphenylalaninemiaSwitzerland
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University Hospital RegensburgCompletedIschemia | Acute Kidney Injury | Fatty Acid-Binding Proteins | Mesenteric Vascular DiseaseGermany
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Swedish Orphan BiovitrumCompletedHereditary Tyrosinemia, Type IGermany, United Kingdom, France
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Cytonet GmbH & Co. KGCRS Clinical Research Services Mannheim GmbHCompleted
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Orphanetics Pharma Entwicklungs GmbHTerminatedPhenylalanine Hydroxylase Deficiencies
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National Center for Research Resources (NCRR)University of TexasCompleted
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University Children's Hospital, ZurichRecruitingUrea Cycle DisordersSwitzerland
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University of Texas Southwestern Medical CenterRecruitingNephrolithiasis, Uric AcidUnited States
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Fondazione SISA (Societa Italiana per lo Studio...Recruiting
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Pascoe Pharmazeutische Praeparate GmbHRecruitingChronic Disease | Acute Disease | Vitamin C DeficiencyGermany
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Barcelona Institute for Global HealthCompletedAttention Deficit Hyperactivity Disorder | Child Behavior Problem | Fatty Acid Deficiency
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Indigo Diabetes NVCompletedDiabetes Mellitus, Type 2 | Diabetes Mellitus | Hypoglycemia | Diabetes Mellitus, Type 1 | Ketoacidosis, Diabetic | Hyperglycaemia (Diabetic)Belgium, Slovenia, France
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Center Trials & TreatmentOleg MartynenkoTerminatedCOVID-19 | SARS-CoV-2 | Furin | RGMc Processing | Paired Basic Amino Acid Cleaving Enzyme (PACE)India, United States, Ukraine
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University Hospital, ToursCompletedAdult Phenylketonuria Non Treated PatientsFrance
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Spanish Society of Internal MedicineCompletedHeart Failure | Decompensated Heart Failure | Acute Heart Failure | Diuretics Drug Reactions | Metabolic AlkalosisSpain
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Swedish Orphan BiovitrumCompletedHereditary Tyrosinemia, Type IBelgium, Denmark, France, Germany, Austria, Czechia, Finland, Hungary, Ireland, Italy, Netherlands, Norway, Poland, Portugal, Spain, Sweden, United Kingdom
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Cycle Pharmaceuticals Ltd.ParexelCompletedHereditary Tyrosinemia, Type ISouth Africa
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Queen's UniversityOntario HIV Treatment NetworkCompletedHIV Infections | Lipodystrophy | AIDS | Lactic AcidosisCanada
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Emory UniversityCompletedDiabetic Ketoacidosis | Ketosis Prone Diabetes | Severe HyperglycemiaUnited States
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Children's National Research InstituteNational Center for Advancing Translational Sciences (NCATS)RecruitingHypoxic-Ischemic Encephalopathy | Urea Cycle Disorder | Organic Acidemia | Fatty Acid Oxidation Disorder | Maple Syrup Urine Disease | Glutaric Acidemia IUnited States
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Andrea GropmanEunice Kennedy Shriver National Institute of Child Health and Human Development... and other collaboratorsRecruitingBrain Diseases, Metabolic, Inborn | Amino Acid Metabolism, Inborn Errors | Urea Cycle DisordersUnited States, Canada, Germany, Switzerland
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Tulane University School of MedicineBioMarin PharmaceuticalCompletedPhenylketonuria | Behavior and Behavior Mechanisms | PAH Gene ExpressionUnited States
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Aeglea BiotherapeuticsCompletedArginase I Deficiency | HyperargininemiaUnited States, Canada, United Kingdom, Portugal
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Dr. Schär AG / SPACompletedPhenylketonurias | Inborn Errors of Metabolism | Metabolic Disease | PKUUnited Kingdom
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Laboratoires GenévrierCompletedVitiligo | PiebaldismBelgium, France, Italy
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Aeglea BiotherapeuticsCompletedArginase I Deficiency | HyperargininemiaUnited States, Canada, United Kingdom, Portugal
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Fondation Ophtalmologique Adolphe de RothschildCompleted
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The Hospital for Sick ChildrenBioMarin PharmaceuticalCompletedPhenylketonuria | Mild HyperphenylalaninemiaCanada
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B. Braun Melsungen AGCompletedPreterm Infants | Parenteral Nutrition n-3 Fatty AcidsGermany
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Kuang Tien General HospitalCompletedMigraine | Omega-3 Polyunsaturated Fatty AcidsTaiwan
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Fondation Ophtalmologique Adolphe de RothschildNot yet recruitingAlbinism, Ocular
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Dr Adnan AghaRecruitingHypothyroidism | Vitamin C Deficiency | Primary HypothyroidismUnited Arab Emirates
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Assiut UniversityNot yet recruitingAKI in Diabetic Ketoacidosis
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University Hospital, BordeauxRecruiting