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Acetyl-L-Carnitine In Severe Hepatic Encephalopathy

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01223768
Enrollment
Unknown
Registered
2010-10-19
Start date
2002-07-31
Completion date
2005-12-31
Last updated
2010-10-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hepatic Encephalopathy (Grade 3 of the West Haven Grading Scale)

Brief summary

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.

Interventions

2g per day

DRUGplacebo

twice per day

Sponsors

University of Catania
Lead SponsorOTHER

Eligibility

Sex/Gender
ALL
Age
40 Years to 65 Years

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

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026