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Study of Bile Acids in Patients With Peroxisomal Disorders
This study is not yet open for participant recruitment.
Study NCT00004442 Information provided by FDA Office of Orphan Products Development
First Received: October 18, 1999 Last Updated: June 23, 2005
History of Changes
Related Studies can be found by searching for the Conditions, Interventions, and Sponsors found in this study:
Conditions listed in this trial
Infantile Refsum's Disease
Zellweger Syndrome
Bifunctional Enzyme Deficiency
Adrenoleukodystrophy
Additional conditions recognized in this trial
Addison Disease
Peroxisomal Disorders
Refsum Disease
Refsum Disease, Infantile
Syndrome
More general conditions related to this trial
Abnormalities, Multiple
Adrenal Gland Diseases
Adrenal Insufficiency
Autoimmune Diseases
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Central Nervous System Diseases
Congenital Abnormalities
Demyelinating Diseases
Digestive System Diseases
Disease
Endocrine System Diseases
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Hereditary Central Nervous System Demyelinating Diseases
Hereditary Motor and Sensory Neuropathies
Heredodegenerative Disorders, Nervous System
Immune System Diseases
Kidney Diseases
Liver Diseases
Mental Retardation
Mental Retardation, X-Linked
Metabolic Diseases
Metabolism, Inborn Errors
Nervous System Diseases
Nervous System Malformations
Neurobehavioral Manifestations
Neurodegenerative Diseases
Neurologic Manifestations
Neuromuscular Diseases
Pathologic Processes
Peripheral Nervous System Diseases
Polyneuropathies
Urologic Diseases
Interventions listed in this trial
chenodeoxycholic acid
cholic acid
ursodiol
Additional drug interventions recognized in this trial
Cholic Acids
More general drug interventions related to this trial
Cathartics
Gastrointestinal Agents
Pharmacologic Actions
Therapeutic Uses
Sponsors listed in this trial
FDA Office of Orphan Products Development
Children's Hospital Medical Center, Cincinnati
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