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Not Yet RecruitingNCT05678309

Establishment of a Patient Library in Patients With Pruritus Sine Materia

Status
Not Yet Recruiting
Phase
Study type
Observational
Enrollment
175 (estimated)
Sponsor
University Hospital, Brest · Academic / Other
Sex
All
Age
18 Years – 99 Years
Healthy volunteers
Not accepted

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.

Detailed description

At inclusion, 52.5 ml of blood will be collected, then an additional skin biopsy and a skin swab. Five questionnaires will be filled in by the patient. At 6 months, then every years for 5 years, the same 5 questionnaires will be collected as well as the clinical data. However, no more biological samples will be collected.

Conditions

Interventions

TypeNameDescription
OTHERBlood samplesAt inclusion : * 52.5 ml of blood : * 24 ml plasma * 20 ml serum * 6 ml DNA * 2.5 ml RNA
OTHERskin swab sampleAt inclusion a skin swab sample will be collected
OTHERskin biopsy sampleAt inclusion a skin biopsy sample will be collected
OTHERQuestionnairesAt 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

Timeline

Start date
2023-04-01
Primary completion
2033-02-01
Completion
2033-02-01
First posted
2023-01-10
Last updated
2023-04-03

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT05678309. Inclusion in this directory is not an endorsement.