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Safety and Efficacy of Meloxicam Compared to Other Nonsteroidal Antiinflammatory Drugs (NSAIDs) in an Observational Cohort Study of Patients With Rheumatoid Arthritis, Osteoarthritis, Lumbago, Scapulohumeral Periarthritis, Neck, Shoulder and Arm Syndrome

Safety and Efficacy of Meloxicam (MOBIC) Compared to Other NSAIDs in Approved Therapeutic Dosages and Routes of Administration in an Observational Cohort Study of Patients With Rheumatoid Arthritis, Osteoarthritis, Lumbago, Scapulohumeral Periarthritis, Neck, Shoulder and Arm Syndrome

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02180516
Enrollment
9984
Registered
2014-07-02
Start date
2001-10-31
Completion date
Unknown
Last updated
2014-07-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Arthritis, Rheumatoid

Brief summary

Study to assess the safety profile of meloxicam by comparing incidence of gastrointestinal adverse events of meloxicam with that of NSAID in the routine daily therapeutic situation.

Interventions

DRUGMeloxicam
DRUGOther Non Steroidal Anti-Inflammatory Drugs (NSAIDs) except etodolac

Sponsors

Boehringer Ingelheim
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Patients with Indications according to the package insert of the prescribed NSAID

Exclusion criteria

* There is no exclusion criterion, because this Post Marketing Study is an observational study

Design outcomes

Primary

MeasureTime frame
Incidence for adverse event of gastrointestinal disorderup to 6 months

Secondary

MeasureTime frame
Incidence for adverse drug reaction of gastrointestinal disorderup to 6 months
Incidence of adverse eventsup to 6 months
Incidence of adverse drug reactionsup to 6 months
Incidence of serious adverse eventsup to 6 months
Incidence for adverse events Perforation, Ulcer and Bleeding (PUB) in the upper gastrointestinal tractup to 6 months

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026