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Determinants of Health Status and Quality of Life in Patients With Primary Immunodeficiencies Inhereted Diagnosed During Childhood (CEREDIH)

P

Public Assistance-Hospitals of Marseille (AP-HM)

Status

Unknown

Conditions

Primary Immune Deficiency

Study type

Observational

Funder types

Other

Identifiers

NCT02868333
2012-A00338-35 (Other Identifier)
2012-10 (Other Identifier)

Details and patient eligibility

About

Background: Most children with primary immune deficiency (PID) now reach adulthood. However, few studies have evaluated their health status and health related quality of life (HRQoL).

Objective: To investigate long-term morbidity, the French Reference Center for PIDs initiated a prospective multicenter cohort: the F-CILC (French Childhood Immune deficiency Long-term Cohort). The data collected will be used to assess the physical health condition of patients who reached adulthood and the impact on their quality of life.

Methods: Patients are asked to complete health status questionnaires. A severity score (grade1 ["mild"] to grade 4 ["life-threatening"]) is assigned to each health condition. The HRQoL of patients is compared to age- and sex-matched French normal values using the SF36 HRQoL questionnaire.

Capsule summary. This will be the first study of adult survivors of childhood PID describing how the burden of health conditions affect their quality of life.

Enrollment

1,780 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patient with primary immune deficiency diagnosed during childhood

Exclusion criteria

  • Patients not willing to answer to quality of life questionnaires

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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