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Establishment of a Patient Library in Patients With Pruritus Sine Materia

NCT05678309 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 175

Last updated 2023-04-03

No results posted yet for this study

Summary

Very little is currently known about the pathophysiology of pruritus sine materia according to the etiology. The creation of this cohort should make it possible to improve our clinical and biological knowledge according to the etiology, by collecting blood, skin, feces, and clinical data.

Conditions

Interventions

OTHER

Blood samples

At inclusion : * 52.5 ml of blood : * 24 ml plasma * 20 ml serum * 6 ml DNA * 2.5 ml RNA

OTHER

skin swab sample

At inclusion a skin swab sample will be collected

OTHER

skin biopsy sample

At inclusion a skin biopsy sample will be collected

OTHER

Questionnaires

At inclusion, at 6 months and every year, the patient will respond to 5 questionnaires : Brest questionnaire, 5-D itch scale, Dermatology Life Quality Index, Itchy Quality of Life and Hospital Anxiety and Depression Scale

Sponsors & Collaborators

  • University Hospital, Brest

    lead OTHER

Eligibility

Min Age
18 Years
Max Age
99 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-04-01
Primary Completion
2033-02-01
Completion
2033-02-01

Countries

  • France

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05678309 on ClinicalTrials.gov