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Utilizing of Physiological Parameters Predict the Prognosis of Cirrhotic Patients With Gastrointestinal Bleeding (SI)

S

St. Martin De Porress Hospital

Status

Enrolling

Conditions

Liver Cirrhosis
Gastrointestinal Bleeding

Treatments

Other: physical indicators such as shock index relatives

Study type

Observational

Funder types

Other

Identifiers

NCT06680583
physical parameters (Registry Identifier)
St. Martin De Porres Hospital

Details and patient eligibility

About

Can physiological indicators such as quick Sequential Organ Failure Assessment , Shock Index, and its derived indicators such as Modified Shock Index , Age Shock Index and Respiratory Adjusted Shock Index accurately predict the prognosis of cirrhosis patients with gastrointestinal bleeding? To explore the improvement of emergency and critical care patient management.

Full description

Cirrhosis is a common chronic liver disease with gastrointestinal bleeding being one of its complications. Gastrointestinal bleeding is quite common in patients with cirrhosis, but its prognosis is difficult to accurately predict. In current clinical practice, critical care physicians often use physiological indicators to assess the risk level of patients. Among them, the Shock Index and its derived indicators such as the Modified Shock Index, Age Shock Index, and Respiratory Adjusted Shock Index have been widely used in other fields, but their actual value in patients with cirrhosis complicated by gastrointestinal bleeding is not yet clear.

The prognosis of cirrhosis patients with gastrointestinal bleeding affects the quality of life and survival of the patients, thus necessitating the establishment of a reliable prognostic assessment tool to assist critical care physicians in making rapid treatment decisions. The motivation of this study is to explore the application value of Shock Index-related indicators in predicting the prognosis of cirrhosis patients with gastrointestinal bleeding, in order to improve the medical efficiency for this specific group of critically ill patients.

Enrollment

150 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria: cirrhosis with gastrointestinal bleeding -

Exclusion Criteria: no complete medical record and trauma patient

-

Trial design

150 participants in 1 patient group

cirrhosis
Description:
cirrhosis with gastrointestinal bleeding
Treatment:
Other: physical indicators such as shock index relatives

Trial contacts and locations

1

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Central trial contact

Chung-Jing Wang, professor; Chia-Hsi Chen, Physician

Data sourced from clinicaltrials.gov

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