Clinical Characteristics of Aquagenic Pruritus in Patients With Myeloproliferative Neoplasms (PASYMPLE)
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|ClinicalTrials.gov Identifier: NCT03688490|
Recruitment Status : Completed
First Posted : September 28, 2018
Last Update Posted : July 1, 2019
Description of the characteristics of aquagenic pruritus expressed by patients suffering from myeloproliferative neoplasms.
Prospective work based on the distribution of a dedicated questionnaire.
|Condition or disease|
Patients with myeloproliferative neoplasms identified and followed in our Institution (Brest University Hospital). Patients could be followed for polycythemia vera or essential thrombocythemia or myelofibrosis.
Distribution of the questionnaire to each patients with myeloproliferative neoplasms (treated or not) suffering from aquagenic pruritus.
Analyse of each characteristic of the aquagenic pruritus by a statistician and publication at the end.
|Study Type :||Observational|
|Actual Enrollment :||70 participants|
|Official Title:||Aquagenic Pruritus Among Patients With Myeloproliferative Syndromes (in English) Prurit Aquagénique Dans Les SYndromes MyéloProLifEratifs (in French)|
|Actual Study Start Date :||July 17, 2013|
|Actual Primary Completion Date :||November 4, 2013|
|Actual Study Completion Date :||November 4, 2013|
- Intensity of the pruritus [ Time Frame: 15 days ]Analogic Visual Scale, from 0 to 10, Worse if >6
- Duration of the pruritus [ Time Frame: 15 days ]Timing expresses in minutes
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03688490
|Principal Investigator:||IANOTTO Jean-Christophe, MD, PhD||Hématologie Clinique-Institut de Cancéro-Hématologie|