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Observational Study of Meloxicam in Mexican Patients With Rheumatic Diseases

Completed
Conditions
Arthritis, Rheumatoid
Interventions
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
GroupInterventionDescription
MeloxicamMeloxicam-
Primary Outcome Measures
NameTimeMethod
Medical global evaluation on a 4-point scale30 and 90 days
Intensity of symptoms at rest evaluated with a 4-point scale30 and 90 days
Intensity of symptoms during movement evaluated with a 4-point scale30 and 90 days
Secondary Outcome Measures
NameTimeMethod
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