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Not yet recruiting NCT07183995

Hematological Disorders in Patients With GI Angiodysplasia

Observational GI Bleeding

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: GI Bleeding. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Hematological Disorders in Patients With Gastrointestinal Angiodysplasia

Overview

The aim of this study will be to assess the association between GIT angiodysplasia with any hematological disorders as von Willebrand factor and Prognostic value of von Willebrand factor on patient's outcomes as risk of rebleeding and hospital mortality

Primary outcome measures

  • Correlation between GIT Angiodysplasia and Hematological disorders [Time frame: Baseline]
Secondary outcome measures (2)
  • Prevelance of different hematological disorders in angiodysplasia patients [Time frame: Baseline]
  • Prognostic value of von Willebrand factor on patient's outcomes as risk of rebleeding and hospital mortality [Time frame: Baseline]

Eligibility criteria

Inclusion criteria

Adults (above 18 years) and elderly Both genders Admitted to GIT Unit with manifestations of GIT bleeding diagnosed by upper endoscopy and Colonoscopy as angiodyplasia.

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Exclusion criteria

other causes of GIT bleeding

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Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Study design

Observational model
Cohort

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07183995 · GI angiodysplasia patients

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗