About this trial
Acute gastrointestinal bleeding is potentially lethal in liver cirrhosis. Accurate assessment of prognosis is critical in a timely fashion. A novel model, CAGIB score, has been developed based on our Chinese multicenter retrospective study. Now, a prospective, international multicenter, observational study will be performed to further compare the performance of CAGIB versus Child-Pugh and MELD scores for evaluating the in-hospital mortality of patients with liver cirrhosis and acute gastrointestinal bleeding.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Patients with liver cirrhosis;
Patients with acute gastrointestinal bleeding presenting with hematemesis, melena, and/or hematochezia;
Adults (age≥18 years old).
Disqualifiers
Components of Child-Pugh, MELD, and CAGIB scores are not available;
In-hospital outcomes are not evaluable.
Trial population
Patients with liver cirrhosis and acute gastrointestinal bleeding
Trial design
Other
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Mortality
Death caused by any events during hospitalizations.
Secondary outcomes
Failure to control bleeding within 5 days
Failure is defined as death or need to change therapy defined by one of the following criteria within 5 days: 1) Fresh hematemesis or nasogastric aspiration of ≥100 ml of fresh blood ≥2 h after the start of a specific drug treatment or therapeutic endoscopy; 2) Development of hypovolaemic shock; 3) 3g drop in hemoglobin (9% drop of hematocrit) within any 24 hours period if no transfusion is administered.
Sponsors and contacts
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Xingshun Qi
Lead sponsor
General Hospital of Shenyang Military Region
Sponsor institution