Arthritis, Rheumatoid
Conditions
Brief summary
Observational study to evaluate the efficacy and safety of meloxicam (Mobicox®) in Mexican population with rheumatic diseases
Interventions
DRUGMeloxicam
Sponsors
Boehringer Ingelheim
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
12 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Age of 12 or older and rheumatologic disease
Exclusion criteria
* Hypersensitivity to meloxicam * Hypersensitivity to other Non-steroidal anti-inflammatory drugs (NSAIDS) * History of asthma, angioedema or urticaria secondary to NSAIDS * Pregnancy or lactation * Recent or current history of peptic ulcer disease, severe renal failure and severe hepatic failure
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Intensity of symptoms at rest evaluated with a 4-point scale | 30 and 90 days |
| Intensity of symptoms during movement evaluated with a 4-point scale | 30 and 90 days |
| Medical global evaluation on a 4-point scale | 30 and 90 days |
Outcome results
None listed