Hepatic Encephalopathy (Grade 3 of the West Haven Grading Scale) Clinical Trial
Verified date | December 2000 |
Source | University of Catania |
Contact | n/a |
Is FDA regulated | No |
Health authority | Italy: Ethics Committee |
Study type | Interventional |
To assess the clinical efficacy of ALC in the treatment of severe hepatic encephalopathy (grade 3 of the West Haven grading scale), we performed a randomised, double blind placebo-controlled study administering ALC to cirrhotic patients, evaluating the effects on ammonia levels and performance in cognitive functions.
Status | Completed |
Enrollment | 0 |
Est. completion date | December 2005 |
Est. primary completion date | |
Accepts healthy volunteers | |
Gender | Both |
Age group | 40 Years to 65 Years |
Eligibility |
Inclusion Criteria: - patients with severe hepatic encephalopathy (grade 3 of the West Haven grading scale) with hepatic cirrhosis Exclusion Criteria: - Patients with a history of recent alcohol abuse, patients using psychotropic drugs (e.g., antipsychotics, interferon, benzodiazepines, anti-epileptics, sedatives and antidepressants) - Other exclusion criteria were the following: major complications of portal hypertension, such as gastrointestinal blood loss, hepatorenal syndrome or bacterial peritonitis; acute superimposed liver injury;patients with metabolic disorders such as diabetes mellitus, unbalanced heart failure and/or respiratory failure or end-stage renal disease; any additional precipitating factors such as high protein intake (additional high-protein meals), constipation; illiteracy. |
N/A
Country | Name | City | State |
---|---|---|---|
Italy | Cannizzaro Hospital | Catania |
Lead Sponsor | Collaborator |
---|---|
University of Catania |
Italy,