Short Term Outcomes in Hospitalized Patients With Liver Cirrhosis

Sponsor
Assiut University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05848414
Collaborator
(none)
100
12

Study Details

Study Description

Brief Summary

This study will be conducted to assess the baseline characteristics and evaluate the 90-day mortality of patients admitted with liver cirrhosis. Also, the study will be done to identify the risk factors of 90-day mortality.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Liver cirrhosis is the end spectrum of all chronic liver diseases characterized by advanced fibrosis, scarring, and formation of regenerative nodules leading to hepatic architectural distortion.

    Liver cirrhosis is a major cause of health burden worldwide. According to the Global Burden of Disease study, liver cirrhosis caused 1.2% of global disability-adjusted life years and 2% of all deaths worldwide in 2010, the 14th leading cause of mortality.

    The progress rate of compensated cirrhosis to decompensated cirrhosis is approximately 58% and once it progresses to decompensated cirrhosis, its mortality rate within 5 years becomes 85% without liver transplantation. Since the progression of cirrhosis is accelerated each time a complication recurs, the management and treatment of the complication are critical in enhancing the quality of life and the life expectancy of patients .

    Post-discharge outcomes are an integral component of healthcare, as they may aid in determining the success and longevity of treatment and how clinicians approach future cases .

    This study will focus on the short-term outcomes of patients hospitalized with liver cirrhosis to provide insight into methods for future healthcare interventions.

    Study Design

    Study Type:
    Observational [Patient Registry]
    Anticipated Enrollment :
    100 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Short Term Outcomes in Hospitalized Patients With Liver Cirrhosis
    Anticipated Study Start Date :
    Jun 7, 2023
    Anticipated Primary Completion Date :
    Jun 7, 2024
    Anticipated Study Completion Date :
    Jun 7, 2024

    Outcome Measures

    Primary Outcome Measures

    1. evaluate the 90-day mortality of patients admitted with liver cirrhosis [90 days]

      Mortality

    Secondary Outcome Measures

    1. identify the risk factors of 90-day mortalit [90 days]

      Risk factors for mortality

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • diagnosis of liver cirrhosis, adult (age ≥ 18 years old) and patients willing to give consent during the selected period.
    Exclusion Criteria:
    • Patients with ages < 18 years or patients that will be lost on follow-up will be excluded from the study.

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • Assiut University

    Investigators

    • Study Director: Ahlam M Farghaly, AhlamGastro2000@yahoo.com

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Esraa Hassan Mohamed kotbey, Doctor, Assiut University
    ClinicalTrials.gov Identifier:
    NCT05848414
    Other Study ID Numbers:
    • Liver cirrhosis mortality
    First Posted:
    May 8, 2023
    Last Update Posted:
    May 8, 2023
    Last Verified:
    Apr 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of May 8, 2023