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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05848414
Other study ID # Liver cirrhosis mortality
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date February 7, 2024
Est. completion date June 7, 2024

Study information

Verified date January 2024
Source Assiut University
Contact Esraa H Kotbey, Resident
Phone 01065186086
Email skotbey1995@gmail.com
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 100
Est. completion date June 7, 2024
Est. primary completion date June 7, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Assiut University

References & Publications (1)

Tsochatzis EA, Bosch J, Burroughs AK. Liver cirrhosis. Lancet. 2014 May 17;383(9930):1749-61. doi: 10.1016/S0140-6736(14)60121-5. Epub 2014 Jan 28. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary evaluate the 90-day mortality of patients admitted with liver cirrhosis Mortality 90 days
Secondary identify the risk factors of 90-day mortalit Risk factors for mortality 90 days
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