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RECRUITING
NCT05928091
NA

Evaluation of the Impact of an Expert Opinion During the Management of Patients With Severe Bleeding on Oral Anticoagulants.

Sponsor: University Hospital, Clermont-Ferrand

View on ClinicalTrials.gov

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

OTHER

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