Von Willebrand Disease (VWD) Clinical Trials

Find Von Willebrand Disease (VWD) Clinical Trials Near You

Algorithm-based Management to Reduce the Recurrence of Gastrointestinal Bleeding and Severe Epistaxis in Von Willebrand Disease: WILL-MANAGE Trial

Status: Recruiting
Location: See all (17) locations...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

WILL MANAGE is a prospective multicenter controlled open label randomized trial comparing an algorithm-based multidisciplinary management to a standard of care to reduce the incidence of bleeding (GI bleeding or severe epistaxis) recurrence in von Willebrand disease.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Males and females adults aged \> 18 years

• With a constitutional von Willebrand Disease (according to the phenotypic criteria of the French Reference Center of von Willebrand Disease)

• With a GI bleeding \[either overt (any hematemesis, any melena or hematochezia with at least a 2g/dL drop in hemoglobin) or occult (iron deficiency anemia with at least 2g/dL drop in hemoglobin)\] with the presence of angiodysplasia or a negative finding on digestive conventional endoscopy OR with a severe epistaxis (requiring red blood cells transfusion or treatment with VWF concentrates)

• Be affiliated to a social security scheme

• Written informed consent obtained

Locations
Other Locations
France
CHU Amiens
NOT_YET_RECRUITING
Amiens
CHRU Brest
NOT_YET_RECRUITING
Brest
Hôpital cardiologique Louis Pradel
NOT_YET_RECRUITING
Bron
CHU Caen
NOT_YET_RECRUITING
Caen
CH Chambery
NOT_YET_RECRUITING
Chambéry
CHU Clermont-Ferrand
NOT_YET_RECRUITING
Clermont-ferrand
CHU Dijon
NOT_YET_RECRUITING
Dijon
AP-HP Hôpital Kremlin Bicetre
NOT_YET_RECRUITING
Le Kremlin-bicêtre
CHU Lille
NOT_YET_RECRUITING
Lille
AP-HM Hôpital Timone
NOT_YET_RECRUITING
Marseille
CHU Montpellier
RECRUITING
Montpellier
CHU Nantes
NOT_YET_RECRUITING
Nantes
CHU Rennes
NOT_YET_RECRUITING
Rennes
CHU Rouen
NOT_YET_RECRUITING
Rouen
CHU Strasbourg
NOT_YET_RECRUITING
Strasbourg
CHU Toulouse
NOT_YET_RECRUITING
Toulouse
CHU Tours
NOT_YET_RECRUITING
Tours
Contact Information
Primary
Marie Caillierez
DRC@chru-lille.Fr
0033320444145
Time Frame
Start Date: 2026-03-10
Estimated Completion Date: 2032-03
Participants
Target number of participants: 66
Treatments
Experimental: Optimized management
systematic gastrointestinal and nasal endoscopic exploration, local endoscopic treatment whenever applicable,prophylaxis with stepwise dose escalation of VWF concentrate and use of antiangiogenic drugs in patients with severe GI angiodysplasia-related bleeding
Other: Standard of care management
Standard of care management
Sponsors
Leads: University Hospital, Lille

This content was sourced from clinicaltrials.gov