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Biobank for Inflammatory Chronic Diseases and Osteoporosis (BIOTOUL)

T

Toulouse University Hospital

Status

Enrolling

Conditions

Osteoporosis
Spondyloarthritis
Psoriatic Arthritis
Rheumatoid Arthritis

Treatments

Biological: Blood sampling

Study type

Observational

Funder types

Other

Identifiers

NCT05039216
RC31/21/0163

Details and patient eligibility

About

The aim of this study is to constitute a biobank for patients followed in the Rheumatology center of Toulouse University Hospital for a chronic inflammatory rheumatism including rheumatoid arthritis (RA), spondyloarthritis(SpA), and psoriatic arthritis (PsA) or a chronic bone disease including osteoporosis in order to identify biomarkers associated with therapeutic response.

Full description

Biologic ant targeted synthetic disease modifying anti-rheumatic drugs (bDMARDs and tsDMARDs) have greatly improved the prognosis of chronic inflammatory diseases. To date, many bDMARDs and tsDMARDs targeting different immunologic mechanisms are available to treat RA, SpA or PsA. However, the choice of the treatment and its mechanism of action is based on physician decision and experience. Indeed, predictive clinical and biological factors associated with therapeutic response that could help the physician to make his/her choice are lacking. The aim of BIOTOUL is to collect and store biologic samples in patients with RA, SpA or PsA who begin a new bDMARD or tsDMARD. This biobank will permit to study several biomarkers and assess the association between such markers and response to therapy.

Furthermore, osteoporosis is a chronic disease leading to fractures and disability. Several ant-osteoporotic drugs are now available and biomarker(s) that would help the physician to choose the best therapeutic sequence are lacking. BIOTOUL will also include patients with osteoporosis to identify biomarkers associated with severity and response to anti-osteoporotic treatments.

Enrollment

2,000 estimated patients

Sex

All

Ages

18 to 99 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Chronic inflammatory rheumatism including RA, SpA or PsA or patients with primary or secondary osteoporosis
  • With National Health Assurance
  • Able to consent to the study

Exclusion criteria

  • Pregnancy or breastfeeding
  • Not able to give a consent
  • Severe anemia (Hb<10g/L)

Trial design

2,000 participants in 2 patient groups

patients initiating a biotherapy or a target treatment
Description:
Blood sampling
Treatment:
Biological: Blood sampling
patients with chronic inflammatory rheumatism, weakening osteopathy or mechanical pathology
Description:
Blood sampling
Treatment:
Biological: Blood sampling

Trial contacts and locations

1

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Central trial contact

Adeline RUYSSEN-WITRAND, MD; Delphine THUILLEZ

Data sourced from clinicaltrials.gov

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