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Completed

NCT Number: NCT02811705

Life Quality Study for PFAPA Patient

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.

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Key information

Conditions

PFAPA Syndrome Marshall syndrome

Age range

2 year–18 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Centre hospitalier de Versailles, Le Chesnay, France

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • PFAPA syndrome patients or FMF patients

Exclusion criteria

  • Participation refusal

Treatment and study plan

Quality of life

Other

Quality of life

Primary outcomes

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

    Time frame: 1 day

Secondary outcomes

  1. Evaluate the fatigue status of patients through questionnaire PedsQL TM 3.0 multidimensional scale tiredness

    Time frame: 1 day

Sponsors and collaborators

Lead sponsor

Versailles Hospital

Other

Registry information

Acronym: PFAPA

Important dates

Study start
2015
Primary completion
2016
Study completion
2017
First posted
Jun 23, 2016
Registry last updated
Feb 8, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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