porphyria due to ALA dehydratase deficiency

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
ELEVATE, a Registry of Patients With Acute Hepatic Porphyria (AHP)	Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Nutritional and Metabolic Diseases, Skin and Connective Tissue Diseases, hepatic porphyria, hereditary coproporphyria, hereditary disease, hereditary skin disorder, liver disorder, metabolic disease, porphyria, porphyria due to ALA dehydratase deficiency, skin disorder	Recruiting	Not stated	2026-10-06		NCT04883905
Evaluating the Prevalence of Acute Hepatic Porphyria in Postural Tachycardia Syndrome	Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Nutritional and Metabolic Diseases, Skin and Connective Tissue Diseases, autonomic nervous system disorder, hepatic porphyria, hereditary coproporphyria, hereditary disease, hereditary skin disorder, liver disorder, metabolic disease, nervous system disorder, orthostatic intolerance, porphyria, porphyria due to ALA dehydratase deficiency, primary dysautonomia, skin disorder	Active, not recruiting	Not stated	2026-09-28		NCT05344599

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