CompletedPhase 3NCT03808805
Aprepitant Versus Hydroxyzine in Persistent Aquagenic Pruritus for Patients With Myeloproliferative Neoplasms
Studying Myeloproliferative neoplasm
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- University Hospital, Brest
- Principal Investigator
- Jean-Christophe IANOTTO, MD, PhDHématologie Clinique-Institut de Cancéro-Hématologie
- Intervention
- Aprepitant 80 mg(drug)
- Enrollment
- 63 target
- Eligibility
- 18 years · All sexes
- Timeline
- 2019 – 2024
Study locations (11)
- CHRU de Brest - Hôpital Morvan, Brest, Brest Cedex, France
- Centre Hospitalier de Cornouaille, Quimper, Quimper, France
- CHU d'Angers, Angers, France
- CHU de Caen, Caen, France
- Centre Hospitalier de Douarnenez, Douarnenez, France
- CHU Grenoble Alpes, Grenoble, France
- Centre Léon Bérard, Lyon, France
- Centre Hospitalier des Pays de Morlaix, Morlaix, France
- CHU de Nantes, Nantes, France
- Hôpital Pontchaillou, Rennes, France
- Hôpital Yves Le Foll, Saint-Brieuc, France
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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