Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2025-12-25 @ 4:18 AM
Ignite Modification Date: 2025-12-25 @ 4:18 AM
NCT ID: NCT02401620
Eligibility Criteria: Inclusion Criteria: 1. Patients over 18 years old. 2. Patients with RA diagnosed according to the standards of the ACR (American College of Rheumatology) in 1987 or to the ACR/EULAR in 2010 3. Patients on treatment with any Rheumatoid Arthritis drug for at least 3 months before their inclusion in the study \* 4. Patients who have provided informed consent prior to taking part in the study. * It's not necessary for patients to be treated in first-line at the moment of the inclusion in the study. Exclusion Criteria: 1. Patients with rheumatic disease other than Rheumatoid Arthritis. Will be exclude patients with the following concomitant diseases: Rheumatic autoimmune disease other than RA; Functional Class IV as defined by the ACR Classification of Functional Status in Rheumatoid Arthritis; Diagnosis of juvenile idiopathic arthritis; inflammatory joint disease other than Rheumatoid Arthritis. 2. Patients with any other concomitant disease or treatment that, under clinical criteria, could affect the results of the study or any major episode of infection or disease requiring hospitalization. 3. Patients with any other medical or physiological condition that, in the view of the investigator, could compromise the ability of the patient to answer the study questions. 4. Patients who participated in interviews of the Phase I (development of the questionnaire)
Healthy Volunteers: False
Sex: ALL
Minimum Age: 18 Years
Study: NCT02401620
Study Brief:
Protocol Section: NCT02401620