Biobank for Inflammatory Chronic Diseases and Osteoporosis
BIOTOUL
1 other identifier
observational
2,000
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Sep 2021
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 6, 2021
CompletedFirst Posted
Study publicly available on registry
September 9, 2021
CompletedStudy Start
First participant enrolled
September 13, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 2, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
September 1, 2031
March 19, 2026
March 1, 2026
5 years
September 6, 2021
March 16, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
EULAR response after 3 months
EULAR response after 3 months
after 3 months
Study Arms (2)
patients initiating a biotherapy or a target treatment
Blood sampling
patients with chronic inflammatory rheumatism, weakening osteopathy or mechanical pathology
Blood sampling
Interventions
4 tubes of 7 mL will be sampled
Eligibility Criteria
monocentric observational longitudinal study
You may qualify if:
- 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
You may not qualify if:
- Pregnancy or breastfeeding
- Not able to give a consent
- Severe anemia (Hb\<10g/L)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Purpan University Hospital
Toulouse, 31059, France
Biospecimen
Blood
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Adeline RUYSSEN-WITRAND, MD
University Hospital, Toulouse
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
September 6, 2021
First Posted
September 9, 2021
Study Start
September 13, 2021
Primary Completion (Estimated)
September 2, 2026
Study Completion (Estimated)
September 1, 2031
Last Updated
March 19, 2026
Record last verified: 2026-03
Data Sharing
- IPD Sharing
- Will not share