Arthritis, Rheumatoid Clinical Trial
Official title:
Clinical and Therapeutic Evaluation of Meloxicam in Mexican Patients With Rheumatic Diseases
NCT number | NCT02184065 |
Other study ID # | 107.272 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | July 3, 2014 |
Last updated | July 8, 2014 |
Start date | January 2004 |
Verified date | July 2014 |
Source | Boehringer Ingelheim |
Contact | n/a |
Is FDA regulated | No |
Health authority | Mexico: Ministry of Health |
Study type | Observational |
Observational study to evaluate the efficacy and safety of meloxicam (Mobicox®) in Mexican population with rheumatic diseases
Status | Completed |
Enrollment | 22639 |
Est. completion date | |
Est. primary completion date | April 2007 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 12 Years and older |
Eligibility |
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 |
Observational Model: Cohort, Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Boehringer Ingelheim |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Intensity of symptoms at rest evaluated with a 4-point scale | 30 and 90 days | No | |
Primary | Intensity of symptoms during movement evaluated with a 4-point scale | 30 and 90 days | No | |
Primary | Medical global evaluation on a 4-point scale | 30 and 90 days | No |
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