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Management of Digestive Haemorrhaging In CHRU of Brest During 2009 and 2014

Risk Factors for Further Bleeding in Patients Admitted to Intensive Care for Gastro Intestinal Bleeding

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03379285
Acronym
HDréa
Enrollment
272
Registered
2017-12-20
Start date
2016-10-03
Completion date
2016-12-31
Last updated
2017-12-20

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

Conditions

Gastro Intestinal Bleeding

Keywords

Gastro Intestinal Bleeding;, Transfusion,, Outcomes

Brief summary

Gastro intestinal (GI) bleeding is relatively frequent and may lead to intensive care unit admission. Although a restrictive strategy for red blood cell transfusion is supported by a large randomized controlled trial literature, less is known about the impact of transfusion strategy of other blood components and administration of anti fibrinolytic on clinical outcomes. This study aims to identify parameters that may be associated with the risk of further bleeding in patients admitted to ICU for GI bleeding.

Interventions

None listed

Sponsors

University Hospital, Brest
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients with Gastro Intestinal Bleeding admitted to either medical or surgical intensive care unit

Exclusion criteria

* patients retrieved from another hospital * age \< 18 years consent withdrawal

Design outcomes

Primary

MeasureTime frameDescription
Bleedingwithin a weekBleeding persistance or recidive requiring an intervention or a scope

Secondary

MeasureTime frameDescription
mortalityduring hospitalisation (28 days)hospital mortality

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026