Life Quality Study for PFAPA Patient

NCT02811705 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 60

Last updated 2023-02-08

No results posted yet for this study

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.

Conditions

  • PFAPA Syndrome

Interventions

OTHER

Quality of life

Quality of life

Sponsors & Collaborators

  • Versailles Hospital

    lead OTHER

Eligibility

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

Timeline & Regulatory

Start
2015-07-31
Primary Completion
2016-12-31
Completion
2017-04-30

Countries

  • France

Study Locations

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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 NCT02811705 on ClinicalTrials.gov