Arthritis, Rheumatoid
Conditions
Brief summary
Evaluation on the amelioration of symptom intensity of the indication and to evaluate drug tolerability.
Interventions
DRUGMeloxicam
tablets or injectable solution
Sponsors
Boehringer Ingelheim
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Healthy volunteers
No
Inclusion criteria
* Patients according to the physicians medical criteria on the labeled indications for Meloxicam
Exclusion criteria
* none
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in assessment of intensity of pain on a 4-point verbal rating scale | up to 1 year |
| Assessment of tolerability on a 4-point scale | up to 1 year |
Secondary
| Measure | Time frame |
|---|---|
| Number of patients with adverse events | up to 1 year |
Outcome results
None listed