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Study identifier: NCT07333144 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Management of Gastrointestinal Bleeding Under Direct Oral Anticoagulants

Condition: Gastrointestinal Bleeding  ·  Sponsor: University Hospital, Strasbourg, France

PhaseN/A
Planned participants250
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Gastrointestinal bleeding (GIB) is a common emergency in hepatology and gastroenterology, with an overall mortality rate ranging from 5% to 10% depending on the study. GIB is classified into two categories: upper GIB (80% of cases) and lower GIB (20% of cases). There are many risk factors for GIB, including anticoagulants. In cases of GD under anticoagulants, there are specific management recommendations. In particular, in cases of severe bleeding under direct oral anticoagulants (DOACs), it is recommended to stop treatment and correct coagulation parameters according to the severity of the bleeding and the associated thrombotic risk. Various treatments can be used for this purpose, including specific antidotes, fresh frozen plasma, and prothrombin complex concentrate (PCC). However, the role of PCC in this indication is uncertain, as is the efficacy and safety data for this drug, due to significant methodological limitations in the few studies conducted on the subject.

This description comes directly from the study's public registry record.

Talk to the study team

Valérie WILME, MD  ·  33 3 88 11 67 68  ·  valerie.wilme@chru-strasbourg.fr

Always discuss trial participation with your own doctor first.

Locations (1)

Service des Urgences Adultes - CHU de Strasbourg - FranceStrasbourg, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT07333144