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Survey of Non-Variceal Upper Gastro Intestinal Bleeding in Vietnamese Patients (NIS-PUB)

AstraZeneca logo

AstraZeneca

Status

Completed

Conditions

Re-bleeding in NVUGIB

Study type

Observational

Funder types

Industry

Identifiers

NCT01292915
NIS-GVN-DUM-2010/1

Details and patient eligibility

About

The main aim of the study is to describes the outcomes of patients with Upper Gastrointestinal Bleed (UGIB) in a real-life setting. Additionally analyse assessed predictors of outcome, including the impact of hemostatic endoscopic and pharmacologic therapies.

Full description

MSD

Enrollment

1,044 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult patients (>=18yrs) admitted to the hospital, or inpatients admitted for another reason, presenting with overt non-variceal upper GI bleed manifesting as hematemesis/coffee ground vomiting, melena, hematochezia...
  • Evidence that an upper GI endoscopy was performed

Exclusion criteria

  • GI bleeding not from NVUGIB

Trial design

1,044 participants in 1 patient group

1

Trial contacts and locations

3

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Data sourced from clinicaltrials.gov

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