Example: Heart Attack
Clinical Trials on Metal Metabolism, Inborn Errors
Total 172 results
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NCT04569604RecruitingConditions: Hypoparathyroidism; Pseudo Hypoparathyroidism
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NCT04551170RecruitingConditions: Pseudohypoparathyroidism; Albright Hereditary Osteodystrophy; Pseudohypoparathyroidism Type 1a
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NCT04537377Not yet recruitingConditions: Wilson's Disease
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NCT04531189Not yet recruitingConditions: Wilson Disease
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NCT04526197Enrolling by invitationConditions: Wilson Disease
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NCT04526210Enrolling by invitationConditions: Wilson Disease
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NCT04422431Not yet recruitingConditions: Wilson Disease
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NCT04419363RecruitingConditions: Rare Diseases; X-linked Hypophosphatemia
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NCT04408300RecruitingConditions: Wilson Disease
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NCT04372446RecruitingConditions: Generalized Arterial Calcification in Infancy; Autosomal Recessive Hypophosphatemic Rickets Type 2
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NCT04337684Enrolling by invitationConditions: Menkes Disease
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NCT04308096Active, not recruitingA Study of KRN23 in Adult and Pediatric Patients With X-linked Hypophosphatemic Rickets/OsteomalaciaConditions: XLH
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NCT04273490RecruitingConditions: X-linked Hypophosphatemia; Hereditary Hypophosphatemia
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NCT04240821Enrolling by invitationConditions: Pseudohypoparathyroidism; Pseudohypoparathyroidism Type 1a; Albright Hereditary Osteodystrophy
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NCT04222452RecruitingConditions: Hypophosphatasia
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NCT04212195RecruitingConditions: Wilson's Disease
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NCT04202965RecruitingConditions: Hereditary Hemochromatosis
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NCT04195763Enrolling by invitationConditions: Hypophosphatasia
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NCT04188964RecruitingConditions: X-linked Hypophosphatemia (XLH)
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NCT04189315WithdrawnConditions: Hypophosphatasia
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NCT04184661Not yet recruitingConditions: Hypophosphatemic Rickets
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NCT04181164RecruitingConditions: Hypophosphatasia (HPP)
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NCT04146935RecruitingConditions: X-linked Hypophosphatemia
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NCT04074512AvailableConditions: Menkes Disease
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NCT04049877Active, not recruitingConditions: X-linked Hypophosphatemia (XLH)
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NCT04018287RecruitingConditions: Hypophosphatasia; Bone Diseases, Metabolic; Bone
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NCT04012658RecruitingConditions: Wilson's Disease
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NCT04006249CompletedConditions: to Evaluate the Prevalence of Periodontal Diseases in Patients With Hemochromatosis at the Time of Diagnosis and / or Their Usual Therapeutic
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NCT03990181Not yet recruitingConditions: Iron Metabolism Disorders; Iron Overload; Polyphenols
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NCT03957720RecruitingConditions: Wilson's Disease
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NCT03920072RecruitingConditions: X-linked Hypophosphatemia
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NCT03879915SuspendedConditions: X-linked Hypophosphatemia
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NCT03867526CompletedConditions: Wilson Disease
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NCT03820518RecruitingConditions: X-linked Hypophosphatemia
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NCT03775187AvailableConditions: X-linked Hypophosphatemia; Tumor-Induced Osteomalacia
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NCT03761290Active, not recruitingConditions: Pseudohypoparathyroidism and Pseudopseudohypoparathyroidism; Pseudohypoparathyroidism Type Ia; Albright Hereditary Osteodystrophy
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NCT03758534RecruitingConditions: Generalized Arterial Calcification in Infancy; Autosomal Recessive Hypophosphatemic Rickets; Pseudoxanthoma Elasticum
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NCT03748966RecruitingConditions: X-linked Hypophosphatemia; Hypophosphatemic Rickets; Hypophosphatemic Rickets, X-Linked Dominant
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NCT03745521RecruitingConditions: X-Linked Hypophosphatemia
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NCT03743272RecruitingConditions: Liver Diseases; Primary Biliary Cirrhosis; Non-Alcoholic Fatty Liver Disease; Non-Alcoholic Steatohepatitis; Cirrhosis; Hemochromatosis; Viral Hepatitis; Autoimmune Hepatitis; Primary Sclerosing Cholangitis
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NCT03718403Not yet recruitingConditions: PHP Ia; PHP IB; Php1C
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NCT03659331Unknown statusConditions: Wilson Disease
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NCT03654794CompletedConditions: Hemochromatosis
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NCT03651505RecruitingConditions: X-linked Hypophosphatemia; Hypophosphatemic Rickets
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NCT03596554RecruitingConditions: X-linked Hypophosphatemia
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NCT03589820Unknown statusConditions: Wilson Disease; Liver Failure
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NCT03581591CompletedConditions: Hypophosphatemia; Hypophosphatemic Rickets; Pain, Chronic
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NCT03539952Active, not recruitingConditions: Wilson Disease
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NCT03489993RecruitingConditions: Hypophosphatemia; X-linked Hypophosphatemia; Renin-angiotensin System; Left Ventricular Hypertrophy
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NCT03478839RecruitingConditions: Generalized Arterial Calcification of Infancy; Autosomal Recessive Hypophosphatemic Rickets Type 2