Overview

PEG (Polyethylene Glycol)Versus Lactulose For Treatment Of Overt Hepatic Encephalopathy

Status:
Unknown status
Trial end date:
2019-12-01
Target enrollment:
0
Participant gender:
All
Summary
The current standard of care for patients with HE includes non-absorbable disaccharides(lactulose);The chemical name for lactulose is 4-O-β-D-galactopyranosyl-D-fructofuranose.The exact mode of action by lactulose is thought to be the conversion to lactic acid and acetic acid by colonic bacteria resulting in acidification of the gut lumen. This favors conversion of ammonia (NH3) to ammonium (NH4+), which is relatively membrane impermeable; therefore, less ammonia is absorbed by the colon. Gut acidification inhibits ammoniagenic coliform bacteria, leading to increased levels of nonammoniagenic lactobacilli. Nonabsorbable disaccharides also work as a cathartic, clearing the gut of ammonia before it can be absorbed.
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Sherief Abd-Elsalam
Treatments:
Lactulose
Criteria
Inclusion Criteria:

- Adult Patients with Overt Hepatic Encephalopathy.

Exclusion Criteria:

1. Patients with active GIT bleeding.

2. Patients with history of bowel obstruction, perforation.

3. Patients with history of allergy to PEG.

4. Treatment with rifaximin or neomycin in the previous 7 days.

5. Patients with major psychiatric illness.

6. Patients receiving benzodiazepines and narcotics.

7. Patients with compromised renal.

8. Patients receiving medications highly bound to plasma proteins eg. Warfarin.

9. Pregnant or lactating women.

10. Fulminant hepatic failure.