CTRI/2024/02/062513
Not yet recruiting
Phase 4
Comparative Effectiveness Of Polyethylene Glycol Electrolyte Solution Versus Lactulose For Treatment Of Hepatic Encephalopathy : A Single Blind, Randomised Control Clinical Trial - NI
I0 sites0 target enrollmentTBD
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- Health Condition 1: F99- Mental disorder, not otherwise specified
- Sponsor
- I
- Status
- Not yet recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\.Patients with any grade of hepatic encephalopathy
- •(grade1\-grade4\)
- •2\.Patients with chronic liver disease and acute on chronic liver failure of any cause.
Exclusion Criteria
- •patients with acute liver failure, suspected intestinal obstruction, pregnancy and lactation, uncontrolled infection and hemodynamically unstable and received more than 1 dose of lactulose prior to enrollment
Outcomes
Primary Outcomes
Not specified
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