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Research line 'Hemophilia, Von Willebrand disease and allied coagulation disorders'

The Van Creveldkliniek holds an international leading position in scientific research in the field of hemophilia, Von Willebrand disease and allied coagulation disorders. This includes innovative therapeutic and gene therapy studies, studies in joint damage, self management and adherence, sports, hemophilia carriers and registries. 

Research includes both studies that are initiated by our researchers and studies that are being performed on behalf of pharmaceutical companies.  An overview of currently active studies at the Van Creveldkliniek is shown in the table below.

StudyPatient populationDescription
2BEGINAdults with severe hemophilia AStudy to detect sub-clinical joint bleeds and arthritis.
DISTRACTIEAdults with hemophilia A and B with severe arthropathy of the ankle Evaluation of the clinical efficacy of ankle joint distraction in hemophilia patients with severe arthropathy of the ankle.
DosEmiHemophiliaPK-guided Hemlibra dose reduction study.
e-ExerciseHemophilia A and BFace-to-face physiotherapy intervention integrated with the use of a mobile app.
EUHASSHemophilia A and BEuropean registry to collect concomitant effects of hemophilia 
FRONTIER-4Hemophilia ALong-term follow-up study to evaluate the safety and efficacy of MIM-8, a factor VIII by-passing agent
HOCUS-POCUSHemophilia A and B and Von Willebrand diseaseAdded value of point of care ultrasound
Hope-BAdults with severe hemophilia B Long-term follow-up study for gene therapy 
HemoNEDAll coagulation disordersDutch registry
HMBeaconGirls (>12 yr) and women with Von Willebrand disease suffering from heavy menstrual bleeding (HMB)Phase II study to investigate safety, tolerability and efficacy of ALN-6400, an siRNA compound directed against plasminogen
PedNetPediatric hemophilia A and BEuropean registry for  inhibitor development
PHYSNET2Hemophilia A and BPredictors of change in physical functioning.
PRIDESPregnant women with Von Willebrand's disease and hemopilia carriersPregnancy and Inherited Bleeding Disorders Study.
RedFlagWomen with Von Willebrand's disease, coagulation factor deficiencies, thrombocytopathies and hemophilia carriersRegistry study for women with heavy menstrual bleeding
XTEND-edChildren with severe hemophilia ATherapeutic study and its long-term follow-up study to the long-half life FVIII product BIVV001
ZEBRHA1Patients with moderate or severe hemophilia A, aged 12 yr and older, who have been on long term prophylaxis and no FVIII inhibitors in the past 3 yearsComparison of NXT007 versus regular FXIII prophylaxis
ZEBRHA2Patients with mild, moderate and severe hemophilia A, with and without FVIII inhibitors, aged 12 yr and olderComparison of NXT007 versus Hemlibra prophylaxis

Cooperation between physiotherapists in haemophilia treatment centers and primary care - Merel Timmer (World Congres Physiotherapy 2021)

Cooperation between physiotherapists in haemophilia treatment centers and primary care - Merel Timmer (World Congres Physiotherapy 2021)

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Do you have any questions about participation in one of our studies? Or do you want to get in touch with one of our researchers? Please feel free to contact the research team of the Van Creveldkliniek. 

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