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Evaluation of the Impact of an Expert Opinion During the Management of Patients With Severe Bleeding on Oral Anticoagulants.
Sponsor: University Hospital, Clermont-Ferrand
Summary
The goal of this randomized clinical trial is to evaluate the impact of an expert opinion during the management of patients with severe bleeding on oral anticoagulants. The main question it aims to answer is : • Does an expert help of decision during the management of patients with severe bleeding is superior to classic management ? The centers will be randomized in one of the two groups : control group and interventional group. Patients will be followed for 3 months. At their inclusion they will be managed in conformity of the randomisation of their center. They will be followed at hour 0 + 6 , H0+24 and at the end of hospitalization. After 3 months, they will be called to assess the occurrence of thrombotic events ou hemorrhage complications. Researchers will compare the classic management versus the management with an expert opinion to see if the expert opinion is superior to classic management.
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
1000
Start Date
2023-10-16
Completion Date
2027-12-31
Last Updated
2025-12-08
Healthy Volunteers
No
Conditions
Interventions
Phone call to an expert team
Patients will be treated as the expert said when the investigator called him
Locations (15)
CH Aurillac
Aurillac, France
CHU de Clermont-Ferrand
Clermont-Ferrand, France
CHU Grenoble
Grenoble, France
CH Le Puy
Le Puy-en-Velay, France
Hospice civils de Lyon
Lyon, France
CH de Montbrison
Montbrison, France
CH Montluçon
Montluçon, France
CH de Moulins
Moulins, France
CHU de Nice
Nice, France
CHR Orléans
Orléans, France
La Pitié-Salpétrière
Paris, France
CHU de Saint-Etienne
Saint-Etienne, France
CHU de Toulouse
Toulouse, France
CHU Tours
Tours, France
CH de Vichy
Vichy, France