Informations générales (source: ClinicalTrials.gov)

NCT01808911 Complet
Outcome of Acquired Haemophilia With Steroid Combined With Cyclophosphamide Versus Steroid Combined With Rituximab (CREHA Study)
Interventional
  • Hémophilie A
Phase 3
University Hospital, Rouen (Voir sur ClinicalTrials)
mai 2012
janvier 2021
02 novembre 2025
CREHA project is a study comparing steroid combined with cyclophosphamide versus steroid combined with rituximab in patients with acquired haemophilia. The study will test the hypothesis that steroid combined with cyclophosphamide is more effective than steroid plus rituximab for FVIII inhibitor eradication in acquired haemophilia.
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Etablissements

Les établissements d'Île-de-France dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données
AP-HP - Hôpital Bicêtre Contact (sur clinicalTrials)
AP-HP - Hôpital Bichat Contact (sur clinicalTrials)
AP-HP - Hôpital Cochin Contact (sur clinicalTrials)
AP-HP - Hôpital Europeen Georges Pompidou Contact (sur clinicalTrials)
AP-HP - Hôpital Henri Mondor-Albert Chenevier Contact (sur clinicalTrials)
AP-HP - Hôpital Jean Verdier Contact (sur clinicalTrials)
Les établissements hors Île-de-France dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données
AP-HM, University Hospital La Conception - 13385 - Marseille 2995469 - France Contact (sur clinicalTrials)
Hospital Archet 1 - 06202 - Nice 2990440 - France Contact (sur clinicalTrials)
Hospital Lyon Sud - 69495 - Pierre-Bénite 2987314 - France Contact (sur clinicalTrials)
Hospital Purpan - 31059 - Toulouse 2972315 - France Contact (sur clinicalTrials)
Hospital Rangueil - 31059 - Toulouse 2972315 - France Contact (sur clinicalTrials)
University Hospital Bocage - 21079 - Dijon 3021372 - France Contact (sur clinicalTrials)
University Hospital G. Montpied - 63003 - Clermont-Ferrand 3024635 - France Contact (sur clinicalTrials)
University Hospital of Bordeaux - Hospital Haut-Lévêque - 33604 - Pessac 2987805 - France Contact (sur clinicalTrials)
University Hospital of Brest - Hospital La cavale Blanche - 29609 - Brest 3030300 - France Contact (sur clinicalTrials)
University Hospital of Nantes, Hospital Hôtel-Dieu - 44093 - Nantes 2990969 - France Contact (sur clinicalTrials)
University Hospital of Poitiers - 86021 - Poitiers 2986495 - France Contact (sur clinicalTrials)
University Hospital of Rouen - 76031 - Rouen 2982652 - France Contact (sur clinicalTrials)
Les établissements sans correspondance certaine dans le répertoire FINESS dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données
Hopsital Bretonneau - 37044 - Tours 2972191 - France Contact (sur clinicalTrials)
Hospital Ambroise Paré - 92104 - Boulogne-Billancourt 3031137 - France Contact (sur clinicalTrials)
Hospital Nord - 42055 - Saint-Etienne 2980291 - France Contact (sur clinicalTrials)
Hospital of Béziers - 34525 - Béziers 3032833 - France Contact (sur clinicalTrials)
Hospital Pitié-Salpêtrière - 75651 - Paris 13 Gobelins 3015772 - France Contact (sur clinicalTrials)
Hospital Saint-Louis - 75475 - Paris 10 Entrepôt 3020216 - France Contact (sur clinicalTrials)
Hospital Sud / Hospital Pontchaillou - 35000 - Rennes 2983990 - France Contact (sur clinicalTrials)
Regional Center of Haemophilia Treatment (CRTH) de Lorraine - Nancy 2990999 - France Contact (sur clinicalTrials)
University Hospital Amiens - 80054 - Amiens 3037854 - France Contact (sur clinicalTrials)
University Hospital Côte de Nacre - 14033 - Caen 3029241 - France Contact (sur clinicalTrials)
University Hospital Michallon - 38043 - Grenoble 3014728 - France Contact (sur clinicalTrials)
University Hospital of Dijon - Hospital Général - 21033 - Dijon 3021372 - France Contact (sur clinicalTrials)
university Hospital of Limoges - 87042 - Limoges 2998286 - France Contact (sur clinicalTrials)
University Hospital Saint-Eloi - 34295 - Montpellier 2992166 - France Contact (sur clinicalTrials)
University Regional Hospital Hautepierre - 67098 - Strasbourg 2973783 - France Contact (sur clinicalTrials)
University Regional Hospital of Lille - 59037 - Lille 2998324 - France Contact (sur clinicalTrials)

Critères

Tous


- men or women

- women post-menpausal or with ongoing contraception

- 18 years old or more

- diagnosis of acquired hemophilia

- patient must be insured

- patient has provided written informed consent prior to enrolment

- patient compliant

Exclusion Criteria:


- constitutional hemophilia

- chemotherapy

- ongoing treatment with prednisone > 20mg further more 1 month

- ongoing treatment with prednisone >0.7 mg/d further more 10 days

- thrombocytopenia

- leukopenia

- chronic disease