Skip to main content
Clinical Trials/NCT02811705
NCT02811705
Completed
Not Applicable

Life Quality Study for PFAPA Patient

Versailles Hospital2 sites in 1 country60 target enrollmentJuly 2015
ConditionsPFAPA Syndrome

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
PFAPA Syndrome
Sponsor
Versailles Hospital
Enrollment
60
Locations
2
Primary Endpoint
Compare quality of life from patients with PFAPA and FMF, reported by parents and by patients themselves
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

This cohort study aims to assess the quality of life (or welfare) related to the health of children and adolescents with an non genetics auto-inflammatory disease PFAPA or Marshall syndrome to compare it to children or adolescents with recurrent fever genetics of Familial Mediterranean fever (FMF) in order to improve their overall care.

Registry
clinicaltrials.gov
Start Date
July 2015
End Date
April 2017
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Versailles Hospital
Responsible Party
Principal Investigator
Principal Investigator

Véronique Hentgen

Dr

Versailles Hospital

Eligibility Criteria

Inclusion Criteria

  • PFAPA syndrome patients or FMF patients

Exclusion Criteria

  • Participation refusal

Outcomes

Primary Outcomes

Compare quality of life from patients with PFAPA and FMF, reported by parents and by patients themselves

Time Frame: 1 day

Secondary Outcomes

  • Evaluate the fatigue status of patients through questionnaire PedsQL TM 3.0 multidimensional scale tiredness(1 day)

Study Sites (2)

Loading locations...

Similar Trials