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Diagnosis and treatment of acute upper gastrointestinal bleeding: a multicenter, cross-sectional, real-world study

Diagnosis and treatment of acute upper gastrointestinal bleeding: a multicenter, cross-sectional, real-world study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500096431
Enrollment
Unknown
Registered
2025-01-23
Start date
2025-03-01
Completion date
Unknown
Last updated
2025-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gastrointestinal bleeding

Interventions

Patients with acute upper gastrointestinal bleeding:NO

Sponsors

Peking Union Medical College Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >=18 years old; 2. Patients diagnosed with acute upper gastrointestinal bleeding.

Exclusion criteria

Exclusion criteria: 1. Acute upper gastrointestinal hemorrhage complicated with lower gastrointestinal hemorrhage; 2. Upper gastrointestinal hemorrhage due to mechanical injury or other trauma; 3. patients who were not considered to be included by other investigators.

Design outcomes

Primary

MeasureTime frame
The total effective rate of acute upper gastrointestinal bleeding;—

Secondary

MeasureTime frame
The amount of allogeneic blood transfusion during the first bleeding period;Medication situation;hospital stay;Re bleeding rate during the same hospitalization;In-hospital all-cause mortality rate;—

Countries

China

Contacts

Public ContactHuadong Zhu

Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College

zhuhuadong1970@126.com+86 139 1069 6435

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026