Nice, France
NCT Number: NCT01566851
Application of EULAR Recommendations for Cardiovascular Risk Management in Patients With Rheumatoid Arthritis
Introduction Cardiovascular diseases are the first cause of death in rheumatoid arthritis (RA). In 2010, EULAR Standing Committee for Clinical Affairs provides 10 recommendations for cardiovascular risk management in patients with rheumatoid arthritis, including a cardiovascular risk assessment annually.
The goal of this study is to evaluate the application of EULAR recommendations in real life in patients with RA in the french population. Inclusion criteria: all patients over 18 years old with rheumatoid arthritis treated with at least one DMARDS and/or biologic therapy, affiliated to the RSI (regime social des independents which correspond to other branches of the universal healthcare insurance agency). Non inclusion criteria: patients declared as rheumatoid arthritis without DMARDS or biologic therapy or treated with steroids alone. The following analysis will be performed on the whole database of the RSI, without name identification. Evaluation criteria: at least once a years the prescription of at least one of the following items use in the evaluation of the cardiovascular risk factors: lipides dosage, glycemia, HbA1C, stress test, Carotid ultra-sonography, coronary or lower limbs arteriography, heart ultra-sonography, cardiology clinic, endocrinology clinic. This evaluation will be done on the whole national population of RSI for the year 2011 (01/01/2011 - 31/12/2011). On a subgroup of patients from the region "Provence Alpes Côte d'Azur", the investigators will analyze the year 2009, and compare to year 2011, to evaluate the impact of theses recommendations.
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Notify MeKey information
Age range
18 year and older
Sex eligibility
All sexes
Study type
Observational
Primary location
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Patients over 18 years, affiliated to RSI, with rheumatoid arthritis treated with at least one DMARDS and/or biologic therapy
Exclusion criteria
- patients under 18 years
- Patients declared as rheumatoid arthritis without DMARDS or biologic therapy or treated with steroids alone
Treatment and study plan
Cardiovascular check-up
OtherCardiovascular check-up once a year in patients with rheumatoid arthritis
Primary outcomes
-
the following items use in the evaluation of the cardiovascular risk factors
Time frame: at time = 2 years
At least once a years the prescription of at least one of the following items use in the evaluation of the cardiovascular risk factors:
- Lipides dosage
- Glycemia
- HbA1C
- Stress test
- Carotid ultra-sonography
- Coronary or lower limbs arteriography
- Heart ultra-sonography
- Cardiology clinic
- Endocrinology clinic
Secondary outcomes
-
the following items use in the evaluation of the cardiovascular risk factors on the sub population
Time frame: t=0 and t=2 years
The same criteria of primary criteria but on the sub population of Povence Alpes Cote-d'Azur region a comparison of these criteria in 2009 (before EULAR recommendations ) and in 2011 (after EULAR recommendations)
Sponsors and collaborators
Lead sponsor
Centre Hospitalier Universitaire de Nice
Other
Registry information
Official study title
Application of EULAR Recommendations for Cardiovascular Risk Management in Patients With Rheumatoid Arthritis in France in the Entire Population of the RSI (Other Branches of the Universal Healthcare Insurance Agency)
Important dates
- Study start
- 2012
- Primary completion
- 2012
- Study completion
- 2013
- First posted
- Mar 29, 2012
- Registry last updated
- Jun 16, 2026
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.