Clinical Trials Directory

Trials / Unknown

UnknownNCT02484573

Evaluation of Intestinal Permeability in Cirrhotic Patients Before and After Treatment With Non-selective Beta Blocker (Propranolol)

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
39 (estimated)
Sponsor
Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

This study seeks to investigate whether non-selective beta blocker treatment decreases intestinal permeability in cirrhotic patients by altering the expression of genes encoding intercellular junction proteins.

Detailed description

There is evidence that the non-selective beta-blocker (NSBB) propranolol reduces intestinal permeability and decreases bacterial translocation in cirrhotic patients, independent of hemodynamic effects on portal pressure. The mechanism by which this decrease in intestinal permeability and bacterial translocation occurs has not been established. Among the proposed mechanisms are: modification of splanchnic hemodynamics, increased gastrointestinal motility, and immunological properties of nonselective beta blockade. It is not known, however, if beta-blocker treatment decreases intestinal permeability by altering the expression of genes encoding intercellular junction proteins. This study seeks to investigate this question to improve understanding of the mechanism by which beta-blockers work in primary and secondary prophylaxis of variceal hemorrhage.

Conditions

Interventions

TypeNameDescription
DRUGPropanolol

Timeline

Start date
2015-05-01
Primary completion
2020-01-01
Completion
2020-08-01
First posted
2015-06-29
Last updated
2019-01-31

Locations

1 site across 1 country: Mexico

Source: ClinicalTrials.gov record NCT02484573. Inclusion in this directory is not an endorsement.