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â??PREVENTION OF HEPATIC ENCEPHALOPATHY IN PATIENTS WITH LIVER CIRRHOSISâ??

Phase 3
Completed
Conditions
Health Condition 1: null- patients with cirrhosis with no previous overt hepatic encephalopathy
Registration Number
CTRI/2012/07/002807
Lead Sponsor
G B Pant Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
100
Inclusion Criteria

Cirrhotic patients, age 18-75 years.

No history of overt hepatic encephalopathy

Exclusion Criteria

Patients on lactulose therapy

History of recent alcohol intake (in past 4 weeks)

Recent infection or antibiotic use (in past 6 weeks)

Patients on secondary prophylaxis for spontaneous bacterial peritonitis

Recent G I bleeding

Hepatocellular carcinoma

Previous TIPS and shunt surgeries

Use of psychotropic drugs which may affect psychometric tests

Any neurologic disease such as Alzheimerâ??s disease, Parkinsonâ??s disease and nonhepatic metabolic encephalopathies

Significant heart, respiratory or renal failure

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
development of overt hepatic encephalopathy in two groupsTimepoint: six months after recruitment of last patient in the study
Secondary Outcome Measures
NameTimeMethod
Baseline psychometric test, critical flicker frequency (CFF), SIBO, oro-cecal transit time and blood ammonia level as predictor of development of hepatic encephalopathy.Timepoint: 6 month after recruitment of last patient
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