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OpenTrials
Completed

NCT Number: NCT04949893

Causes of Chronic Pruritus

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

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Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

CHRU de Brest

Brest, 29609, France

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Primary outcomes

  1. Causes of chronic pruritus

    Time frame: 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)

Sponsors and collaborators

Lead sponsor

University Hospital, Brest

Other

Registry information

Official study title

Causes of Chronic Pruritus: a Retrospective Study

Acronym: PRURISINE

Important dates

Study start
2019
Primary completion
2019
Study completion
2019
First posted
Jul 2, 2021
Registry last updated
Jul 2, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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