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Efficacy and Safety Study of Ammonul® in Patients With Grade 3 or 4 Hepatic Encephalopathy
This study has been terminated.
( Study was terminated due to lack of enrollment and businesss decisions. )
Study NCT00597909 Information provided by Hyperion Therapeutics, Inc.
First Received: January 9, 2008 Last Updated: July 14, 2009
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
Hepatic Encephalopathy
Additional conditions recognized in this trial
Brain Damage, Chronic
Delirium
Encephalitis
Neurotoxicity Syndromes
More general conditions related to this trial
Brain Diseases
Brain Diseases, Metabolic
Central Nervous System Diseases
Central Nervous System Infections
Central Nervous System Viral Diseases
Confusion
Delirium, Dementia, Amnestic, Cognitive Disorders
Digestive System Diseases
Disorders of Environmental Origin
Hepatic Insufficiency
Liver Diseases
Liver Failure
Mental Disorders
Metabolic Diseases
Nervous System Diseases
Neurobehavioral Manifestations
Neurologic Manifestations
Poisoning
Signs and Symptoms
Virus Diseases
Interventions listed in this trial
placebo solution (10% dextrose)
Additional drug interventions recognized in this trial
Benzoates
Phenylacetic acid
Sodium Benzoate
More general drug interventions related to this trial
Anti-Infective Agents
Antifungal Agents
Antimetabolites
Antimetabolites, Antineoplastic
Antineoplastic Agents
Molecular Mechanisms of Pharmacological Action
Pharmacologic Actions
Therapeutic Uses
Sponsors listed in this trial
Hyperion Therapeutics, Inc.
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