Clinical Trials Directory

Trials / Unknown

UnknownNCT04142723

Alcoholic Hepatitis in Latin-America: A Prospective and Multicentric Study (AH-LATIN).

Status
Unknown
Phase
Study type
Observational
Enrollment
1,000 (estimated)
Sponsor
Pontificia Universidad Catolica de Chile · Academic / Other
Sex
All
Age
18 Years – 99 Years
Healthy volunteers
Not accepted

Summary

The primary objective of this study is to determine the prevalence of AH in addition to its clinical characteristics and in-hospital mortality of patients that are hospitalized for AH in different hospitals across Latin American countries This study is carried out in different health centers throughout America, with all the countries belonging to the Latin American Association for the study of liver diseases (ALEH) more Canada and United States This would allow us to better understand the epidemiology of AH in our region and thus implement prevention measures with more solid data. Importantly, this would allow us to optimize therapeutic measures

Detailed description

This study is sponsored and organized by the "group Latin American of interest special in the study of the disease hepatic Alcohol" (ALEH-GLEHA), belonging to the Latin American Association for the study of the hepatic illnesses (ALEH), which is an association non-profit that has nearly 1,000 members from most of the countries of Latin America. All patients admitted to the hospital with suspected alcoholic hepatitis will be evaluated to see if they can be included in the study. Patients will be enrolled according with the inclusion and exclusion criteria. The investigators will take a blood sample to be analyzed as part of the necessary data record, for the study of genes and identification of proteins involved in the development, evolution and prognosis of alcoholic hepatitis. If the medical doctor had instructed to perform a liver biopsy, voluntarily the investigators will ask to participants donate a small share of the surplus of histological sample To achieve this, it is necessary to generate a data bank of clinical information and biological samples (blood, urine, bile, stools, salivary sample or tissue samples) that allows studying the various factors involved in the development and prognosis of this disease in the countries of the Americas. The investigators will make a clinical follow-up for a year, consisting of phone calls to complete a questionnaire about participant's health. These calls will be made in month 1, 3, 6 and 12 subsequent to participant's hospital discharge. The data collected are identified by a code and only the study physicians can correlate the data with the participants and medical history, so the participant's identity will not be shared. There is no financial compensation associated with the study

Conditions

Interventions

TypeNameDescription
BIOLOGICALblood withdrawvenous blood sampling

Timeline

Start date
2019-06-20
Primary completion
2022-06-20
Completion
2022-06-20
First posted
2019-10-29
Last updated
2019-10-29

Locations

1 site across 1 country: Chile

Source: ClinicalTrials.gov record NCT04142723. Inclusion in this directory is not an endorsement.