Actively Recruiting
Utilizing Physiological Parameters and Derived Indices to Predict Prognosis in Cirrhotic Patients with Gastrointestinal Bleeding
Led by St. Martin De Porress Hospital · Updated on 2026-03-17
150
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to evaluate whether physiological indicators like the quick Sequential Organ Failure Assessment, Shock Index, and related measures such as the Modified Shock Index, Age Shock Index, and Respiratory Adjusted Shock Index can accurately predict the outlook for patients with liver cirrhosis who experience gastrointestinal bleeding. Cirrhosis is a common chronic liver disease, and gastrointestinal bleeding is a serious complication with an uncertain prognosis. Developing reliable tools to assess risk can help improve emergency and critical care management for these patients. The study will observe and analyze the use of these physiological parameters in cirrhosis patients with gastrointestinal bleeding to understand their value in predicting patient outcomes. No specific treatment is given as this is an observational study focusing on assessing these indicators. Data will be collected throughout the study, which is expected to last an average of six months from the start date. Participants will be monitored using measures such as heart rate, blood pressure, and respiratory rate to calculate the Shock Index and its derivatives. Researchers will use these indicators to predict prognosis and assist in rapid treatment decisions. Study data will be gathered continuously until the study's completion, helping to improve medical care efficiency for critically ill cirrhosis patients with gastrointestinal bleeding.
CONDITIONS
Brief Title
Utilizing of Physiological Parameters Predict the Prognosis of Cirrhotic Patients With Gastrointestinal Bleeding
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of cirrhosis with gastrointestinal bleeding
You will not qualify if you...
- Incomplete medical records
- Recent trauma injury
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 6 months
Participants with cirrhosis and gastrointestinal bleeding are observed to assess physiological parameters such as shock index and related indicators to predict prognosis.
Regular assessments during hospital stay and follow-up visits as determined by clinical care
Trial Site Locations
Total: 1 location
1
St. Martin De Porres Hospital
Tainan, Taiwan, 60069
Actively Recruiting
Research Team
C
Chia-Hsi Chen, Physician
C
Chung-Jing Wang, professor
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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