Osteoarthritis
Conditions
Brief summary
Study to evaluate the efficacy and safety of meloxicam (Mobicox®) in Mexican population with rheumatic diseases.
Interventions
None listed
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
* none
Exclusion criteria
* Hypersensitivity to meloxicam or to other NSAIDS * History of asthma, angioedema or urticaria secondary to NSAIDS * Pregnancy or lactation * Recent or current history of peptic ulcer disease, severe renal failure, severe hepatic failure * Age below of 12 years.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in intensity of the symptoms measured with a four-point scale | Baseline, 30 and 90 days |
Secondary
| Measure | Time frame |
|---|---|
| Number of patients with adverse events | up to 90 days |
| Degree of satisfaction evaluated with a six point numerical rating scale | up to 90 days |
Outcome results
None listed