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PRURISINE: Causes of Chronic Pruritus

Sponsor
University Hospital, Brest (Other)
Overall Status
Completed
CT.gov ID
NCT04949893
Collaborator
(none)
200
Enrollment
1
Location
5
Actual Duration (Months)
39.8
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

The aim of this study is to include all patients followed between 2008 and 2018 in order to analyze the etiologie of the chronic pruritus

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    200 participants
    Observational Model:
    Cohort
    Time Perspective:
    Retrospective
    Official Title:
    Causes of Chronic Pruritus: a Retrospective Study
    Actual Study Start Date :
    May 2, 2019
    Actual Primary Completion Date :
    Oct 2, 2019
    Actual Study Completion Date :
    Oct 2, 2019

    Outcome Measures

    Primary Outcome Measures

    1. Causes of chronic pruritus [through study completion, an average of 1 year]

      Analyze the etiology of chronic pruritus : uremic pruritus, cholestatic pruritus, haematologic pruritus, metabolic pruritus, neuropathic pruritus, psychogenic pruritus, idiopathic pruritus thanks to results of biological parameters, Imaging data, clinical data (for example consultation with psychiatric for psychogenic pruritus)

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:

    • more than 18 years old

    • In patient in a day hospital or longer hospitalization in the dermatology department

    • With chronic pruritus which means pruritus longer than 6 weeks without skin lesions specific to pruritic dermatitis.

    Exclusion Criteria:

    • Itchy dermatose

    • Refusal to particpate

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 CHRU de Brest Brest France 29609

    Sponsors and Collaborators

    • University Hospital, Brest

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University Hospital, Brest
    ClinicalTrials.gov Identifier:
    NCT04949893
    Other Study ID Numbers:
    • PRURI SINE (29BRC18.0247)
    First Posted:
    Jul 2, 2021
    Last Update Posted:
    Jul 2, 2021
    Last Verified:
    Jul 1, 2021
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:
    Pruritus

    Study Results

    No Results Posted as of Jul 2, 2021