Predictors of Decompensation, Acute-on-chronic Liver Failure and Mortality in Liver Cirrhosis
Recruiting now
Conditions studied: Cirrhosis and Chronic Liver Disease
In brief
The purpose of this study is to identify factors that predict the development of decompensation, acute-on-chronic liver failure (ACLF) and death in patients with liver cirrhosis. Clinical data will be retrieved from existing hospital records. This information may help doctors to identify patients with cirrhosis who are at risk of deterioration earlier (before they develop complications) and to develop effective treatment strategies to prevent or delay these complications. This study is designed as a prospective, non-interventional, observational study. This means that if you agree to participate in the study, you will not be required to undergo any additional hospital visits, tests, procedures or interventions other than the usual standard-of-care management that your doctor will provide. If you consent to participate in this study, you will be providing the study investigators permission to review and analyse your clinical data from the hospital clinical records. Your data will be collected throughout the course of your disease until liver transplantation or death.
Key facts
- Study ID
- NCT07438288
- Run by
- Singapore General Hospital
- People needed
- 2200
- Starts
- 2022-08-12
- Expected to finish
- 2032-08-12
- Last updated by the study team
- 2026-02-27
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients with clinical diagnosis of liver cirrhosis
- Age 18 years and above (parental consent required if below 21 years)
- Willing and able to provide informed consent
You may not qualify if…
- No clinical evidence of liver cirrhosis
- Not willing to provide informed consent
Where it is running
- Changi General Hospital — Singapore, Singapore (enrolling)
- Sengkang General Hospital — Singapore, Singapore (enrolling)
- Singapore General Hospital — Singapore, Singapore (enrolling)
Full record on ClinicalTrials.gov
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