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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05986825
Other study ID # 29BRC22.0225 (QUALIVER)
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date August 29, 2023
Est. completion date September 2024

Study information

Verified date August 2023
Source University Hospital, Brest
Contact Emilie BRENAUT, PH
Phone +33298223315
Email emilie.brenaut@univ-brest.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Validation of the French Version of the Score on Quality of Life in Hidradenitis Suppurativa. The French HiSQOL will be completed by 60 patients with hidradenitis suppurativa a first time, and a second time 1 week later.


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date September 2024
Est. primary completion date September 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Age =18 years - Patient with Verneuil disease - Beneficiary of or affiliated to a social security insurance - Participation agreement Exclusion Criteria: - Patients physically or mentally unable to complete questionnaires. - Refusal to participate - Patient under legal protection (guardianship, curatorship) or deprived of liberty

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Verneuil questionnaire Validation
Request patient to Complete the questionnaire for validation of the French version

Locations

Country Name City State
France CHU Brest Brest

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Brest

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Validation of the questionnaire During the visit and 1 week later
See also
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