effect of probiotic in cirrhosis patients
Phase 3
Recruiting
- Conditions
- Cirrhosis.Fibrosis and cirrhosis of liver
- Registration Number
- IRCT20190306042944N1
- Lead Sponsor
- Ahvaz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 80
Inclusion Criteria
cirrhosis with any reasons
Age above 18
Exclusion Criteria
Chronic physical or sychiatric illness
Encephalopathy
Active infection
Addiction
Intake immunosuppressive drugs
Patient Dissatisfaction
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Quality of life in cirrhosis patients. Timepoint: At the beginning of the study and 3 months later (end of the study). Method of measurement: According to the quality of life questionnaire for chronic liver patients (CLDQ).
- Secondary Outcome Measures
Name Time Method