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Validation of the French Version of the CQR (Compliance Questionnaire Rheumatology) (CQR-F)

C

Centre Hospitalier Universitaire de Nīmes

Status

Enrolling

Conditions

Rheumatoid Polyarthritis

Treatments

Other: Questionnaire

Study type

Observational

Funder types

Other

Identifiers

NCT03642795
PHRCI/2016/CGV-01

Details and patient eligibility

About

The purpose of this study is to develop a French language version of the Compliance-Questionnaire-Rheumatology for use in French and Francophone rheumatology services

Enrollment

150 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • The patient must have given their free and informed consent and signed the consent form
  • The patient must be a member or beneficiary of a health insurance plan
  • The patient is at least 18 years old
  • The patient has rheumatoid polyarthritis as defined by the ACR-EULAR 2010 criteria, treated orally or subcutaneously with MTX for at least 3 months with a stable (unchanged) dosage for at least 1 month, and a stable (unchanged) route of administration for at least 1 month. And no planned change in Methotrexate intake at least until the second study visit. Other treatments at the same time are authorized

Exclusion criteria

  • The subject is participating in an interventional study, or is in a period of exclusion determined by a previous study
  • The subject refuses to sign the consent
  • It is impossible to give the subject informed information
  • The patient is under safeguard of justice or state guardianship
  • The subject has a contraindication to taking methotrexate (including a patient with a desire to become pregnant).

Trial design

150 participants in 1 patient group

Patients with rheumatoid polyarthritis
Treatment:
Other: Questionnaire

Trial contacts and locations

4

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Central trial contact

Cécile Gaujoux Viala, MD

Data sourced from clinicaltrials.gov

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