Actively Recruiting

Age: 18Years +
All Genders
NCT07089277

External Validation of the Glasgow-Blatchford Bleeding Score in a Tunisian Population

Led by Hôpital Universitaire Sahloul · Updated on 2025-07-28

250

Participants Needed

1

Research Sites

104 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study aims to externally validate the Glasgow-Blatchford Score (GBS) in a Tunisian population presenting with non-traumatic upper gastrointestinal bleeding. Despite advances in endoscopic management, early risk stratification remains essential to guide clinical decision-making. In Tunisia, the routine hospitalization of all patients for observation presents a challenge, highlighting the need for reliable prognostic tools. The study is designed as a multicenter, descriptive, and analytical investigation across several emergency departments. Adult patients (≥16 years) will be included, with follow-up conducted at 30 days to assess for adverse outcomes including rebleeding, the need for hemostasis, complications, and mortality. Clinical and epidemiological data will be collected using a standardized form. Statistical analysis will evaluate the predictive performance of the GBS, focusing on sensitivity, specificity, and predictive values for 30-day outcomes. The results are expected to determine whether GBS is a valid and useful tool for risk assessment in the Tunisian context, potentially aiding in more efficient and targeted patient management.

CONDITIONS

Official Title

External Validation of the Glasgow-Blatchford Bleeding Score in a Tunisian Population

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult patients (18 years or older) presenting with non-traumatic upper gastrointestinal bleeding
Not Eligible

You will not qualify if you...

  • Patients under 18 years of age
  • Diagnosis of external hemorrhoids with mucosal lesions
  • Patients who do not consent to participate
  • Patients lost to follow-up or with incomplete data

AI-Screening

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Trial Site Locations

Total: 1 location

1

Sahloul University Hospital

Sousse, Tunisia, 4021

Actively Recruiting

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Research Team

R

Riadh Boukef, Professor

CONTACT

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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