Observational Study of Meloxicam in Mexican Patients With Rheumatic Diseases
- Registration Number
- NCT02184065
- Lead Sponsor
- Boehringer Ingelheim
- Brief Summary
Observational study to evaluate the efficacy and safety of meloxicam (Mobicox®) in Mexican population with rheumatic diseases
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 22639
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
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Meloxicam Meloxicam -
- Primary Outcome Measures
Name Time Method Medical global evaluation on a 4-point scale 30 and 90 days 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
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What are the molecular mechanisms of meloxicam in rheumatoid arthritis treatment?
How does meloxicam compare to NSAIDs like diclofenac in managing rheumatic diseases?
Which biomarkers correlate with meloxicam response in Mexican rheumatoid arthritis patients?
What adverse events are associated with meloxicam in large rheumatoid arthritis cohorts?
Are there combination therapies involving meloxicam for refractory rheumatoid arthritis cases?