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French Adult Primary Immune Thrombocytopenia

Conditions
Thrombocytopenia
Interventions
Other: Medical information
Registration Number
NCT03429660
Lead Sponsor
University Hospital, Toulouse
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.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
10000
Inclusion Criteria
  • Incident case of immune thrombocytopenia or control patient
Exclusion Criteria
  • Patient not registered in the database between 2009 and 2012

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
CohortMedical informationData to be collected are : - Medical information on Immune Thrombocytopenia treatment
Primary Outcome Measures
NameTimeMethod
Exposition or non exposition to available immune thrombocytopenia persistentup to 10 years

Data will be extracted until the end of study

Secondary Outcome Measures
NameTimeMethod
Mortality as assessed date of death collected in the databaseEach year until 10 years

Data will be extracted every year of the study until the end of study

Number of hospitalization for bleeding in the databaseEach year until 10 years

Number of hospitalization for bleeding will be extract from database every year

Safety of treatment for cardio-vascular eventsEach year until 10 years

Number of hospitalization for cardio-vascular events will be extract from database every year

Safety of treatment for thrombo-embolic eventsEach year until 10 years

Number of hospitalization for thrombo-embolic events will be extract from database every year

Safety of treatment for infectionsEach year until 10 years

Number of infections is represented by number of hospitalization and antibiotics dispensation and will be extract from database every year

Trial Locations

Locations (1)

University Hospital of Toulouse

🇫🇷

Toulouse, France

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