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Search / Trial NCT01722617

A Study to Validate Questionnaires FLARE and OM-RA-FLARE Measuring Disease Flares in Patients With Rheumatoid Arthritis.

Launched by CENTRAL HOSPITAL, NANCY, FRANCE · Nov 5, 2012

Trial Information

Current as of May 17, 2025

Completed

Keywords

ClinConnect Summary

There will be 6 months of follow up including 3 medical visits for each patients:

* M0 (medical visit for inclusion)
* follow up between M0 - M3
* M3 (medical visit at 3 months after inclusion)
* follow up between M3 - M6
* M6 (medical visit at 6 months after inclusion)

At the inclusion visit (M0), after the verification of inclusion and non-inclusion criteria, the following information will be collected:

* Socio-demographical data : age, sex, level of education (primary, secondary, college, university), occupational category (INSEE in 6 categories)
* Items of the ACR 1987 and ACR/EULAR ...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Age ≥ 18 years;
  • Having Rheumatoid Arthritis (RA) since more than 6 months, meeting the ACR 1987 and the ACR / EULAR 2010;
  • * Treatment of RA:
  • Treatment of disease modifying anti-rheumatic drugs (DRMADs) or biological treatment stable for more than 2 months;
  • Symptomatic treatment (including corticosteroid) stable for more than 2 months;
  • Receive the medical exam first;
  • Agreed and signed the informed consent form;
  • Ability to comply with the study protocol;
  • Having the social insurance coverage
  • Exclusion Criteria:
  • Patients undergoing surgery during the study period;
  • Patients without any affiliation to a social security coverage (or entitled beneficiary);
  • Patients under guardianship or trusteeship.

About Central Hospital, Nancy, France

Central Hospital, located in Nancy, France, is a leading healthcare institution dedicated to advancing medical research and improving patient outcomes. As a prominent clinical trial sponsor, the hospital is committed to conducting innovative studies across various therapeutic areas, fostering collaboration among multidisciplinary teams of healthcare professionals and researchers. With a strong emphasis on ethical standards and patient safety, Central Hospital leverages its state-of-the-art facilities and expertise to contribute to the development of cutting-edge treatments and enhance the overall quality of care within the community and beyond.

Locations

Dijon, Bourgogne, France

Brest, Bretagne, France

Nantes, Bretagne, France

Besançon, Franche Comté, France

Fort De France, La Martinique, France

Rouen, Normandie, France

Grenoble, Rhône Alpes, France

Marseille, , France

Montpellier, , France

Paris, , France

Paris, , France

Poitiers, , France

Toulouse, , France

Patients applied

0 patients applied

Trial Officials

Francis Guillemin, MD, PhD

Principal Investigator

CIC-EC Inserm, CHU de Nancy

Bruno Fautrel, MD, PhD

Principal Investigator

Service de Rhumatologie, Groupe Hospitalier Pitié - Salpêtrière, Paris

Jacques Morel, MD, PhD

Principal Investigator

Service d'immunorhumatologie, Hôpital Lapeyronie, Montpellier

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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