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French Adult Primary Immune Thrombocytopenia

French Adult Primary Immune Thrombocytopenia: a pHarmacoepidemiological Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03429660
Acronym
FAITH
Enrollment
10000
Registered
2018-02-12
Start date
2013-10-31
Completion date
2023-05-31
Last updated
2020-10-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Thrombocytopenia

Keywords

Disease epidemiology, Risk assessment, Drug utilisation study, Effectiveness evaluation

Brief summary

Primary immune thrombocytopenia (ITP) is rare. First-line treatment is corticotherapy. Then, several second-line treatments (SLT) are available: splenectomy, off-label rituximab and thrombopoietin-receptor agonists since 2009. The compared efficacy and safety on clinical events in the long-term are unknown. The main objective of the FAITH study is to build the cohort of all treated adult persistent (≥3 months) primary ITP patients in France, to assess the benefit-to-risk ratio of SLT in real-life practice. Data source is the database of French Health Insurance System (SNIIRAM) which covers the entire French population. It collects demographic, chronic disease, hospitalization and drug dispensing data. All patients with ITP were extracted from 2009 to 2012, and then every year for 10 years. The investigator will build the cohort from raw data. Outcomes (death, hospitalization, drug dispensing) will be compared according to SLT, with controls from the general population and untreated patients.

Interventions

OTHERMedical information

The information collected are about : * Introduction or non-introduction of treatment * Cumulative dose of treatment * Drug dispensation and withdrawal * Hospitalization reason * Safety information * Demographic data (date of death)

Sponsors

University Hospital, Toulouse
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Incident case of immune thrombocytopenia or control patient

Exclusion criteria

* Patient not registered in the database between 2009 and 2012

Design outcomes

Primary

MeasureTime frameDescription
Exposition or non exposition to available immune thrombocytopenia persistentup to 10 yearsData will be extracted until the end of study

Secondary

MeasureTime frameDescription
Mortality as assessed date of death collected in the databaseEach year until 10 yearsData will be extracted every year of the study until the end of study
Number of hospitalization for bleeding in the databaseEach year until 10 yearsNumber of hospitalization for bleeding will be extract from database every year
Safety of treatment for infectionsEach year until 10 yearsNumber of infections is represented by number of hospitalization and antibiotics dispensation and will be extract from database every year
Safety of treatment for cardio-vascular eventsEach year until 10 yearsNumber of hospitalization for cardio-vascular events will be extract from database every year
Safety of treatment for thrombo-embolic eventsEach year until 10 yearsNumber of hospitalization for thrombo-embolic events will be extract from database every year

Countries

France

Contacts

Primary ContactMaryse LAPEYRE-MESTRE, PHD
maryse.lapeyre-mestre@univ-tlse3.fr

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 23, 2026