Skip to content

12-Week No-Rofecoxib Plus Aspirin Endoscopy Study (0782-003)

Status
Terminated
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00543465
Enrollment
49
Registered
2007-10-15
Start date
2004-08-31
Completion date
2004-11-30
Last updated
2015-06-02

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

Conditions

Arthritis, Rheumatoid, Osteoarthritis

Brief summary

This study will look at the incidence of gastric and/or duodenal ulcers in patients with osteoarthritis or rheumatoid arthritis in four different treatment groups (a) MK0782 21 mg plus enteric-coated aspirin, (b) MK0782 42 mg plus enteric-coated aspirin, (c) celecoxib 200 mg plus enteric-coated aspirin, and enteric-coated aspiring alone. This is an early phase trial and some specific protocol information is in progress and not publicly available at this time. (Full information is available to trial participants).

Interventions

DRUGMK0782

Sponsors

Merck Sharp & Dohme LLC
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
45 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Has osteoarthritis or rheumatoid arthritis for at least 6 months prior to start of study * Osteoarthritis (OA): must have diagnosis of OA in knee, hip, hand or spine Patient is not on chronic aspirin therapy (taking aspirin at any dose, on a daily basis, for a minimum of 4 weeks prior to Visit 2 for any medical condition * Must be willing to limit alcohol use to no more than 2 drinks per day * Avoid strenuous physical activity

Exclusion criteria

* Mentally or legally incapacitated * Has systemic lupus erythematosus, Paget's disease * Has a history of esophageal, gastric biliary, or small intestine surgery (hiatal surgeries and any GI surgery that causes clinical malabsorption or delayed gastric emptying * Has uncontrolled hypertension * Has uncontrolled diabetes * Has had heart attack, unstable angina, coronary angioplasty, stent placement, coronary artery bypass grafting in the last 6 months * Has congestive heart failure * Has had active liver disease within the last 2 years

Outcome results

None listed

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