Using physiological parameters to predict outcomes in cirrhotic patients with gastrointestinal bleeding
Utilizing of Physiological Parameters And Derived Indices to Predict The Prognosis of Cirrhotic Patients With Gastrointestinal Bleeding
This study is testing if certain health measurements can help doctors predict how well patients with liver cirrhosis and gastrointestinal bleeding will do, so they can provide better emergency care.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 150 (estimated) |
| Sex | All |
| Sponsor | St. Martin De Porress Hospital Academic / other |
| Locations | 1 site (Tainan) |
| Trial ID | NCT06680583 on ClinicalTrials.gov |
What this trial studies
This observational study aims to evaluate whether physiological indicators, such as the Shock Index and its variations, can accurately predict the prognosis of patients with liver cirrhosis experiencing gastrointestinal bleeding. By analyzing these indicators, the study seeks to enhance the management of emergency and critical care for this patient population. The research focuses on the application of established physiological measures to improve treatment decision-making in critical situations. The ultimate goal is to develop a reliable prognostic tool that can assist healthcare providers in delivering timely and effective care.
Who should consider this trial
Good fit: Ideal candidates for this study are patients diagnosed with liver cirrhosis who are experiencing gastrointestinal bleeding.
Not a fit: Patients without complete medical records or those who have sustained trauma may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved prognostic assessments and better management strategies for cirrhotic patients facing gastrointestinal bleeding.
How similar studies have performed: While the use of physiological indicators like the Shock Index has been successful in other medical fields, their specific application in cirrhotic patients with gastrointestinal bleeding remains largely untested.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: cirrhosis with gastrointestinal bleeding - Exclusion Criteria: no complete medical record and trauma patient \-
Where this trial is running
Tainan
- St. Martin De Porres Hospital — Tainan, Taiwan (Recruiting)
Study contacts
- Study coordinator: Chia-Hsi Chen, Physician
- Email: urologist3509@gmail.com
- Phone: 886-5-2756000
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.