NCT Number: NCT00157872
A Study of Rofecoxib Versus Naproxen in the Treatment of Chinese Patient With Rheumatoid Arthritis (0966-231)
A study to compare rofecoxib versus naproxen in the treatment of Chinese patients with rheumatoid arthritis.
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Notify MeKey information
Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 4
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Chinese males or females at least 18 years of age with rheumatoid arthritis
Treatment and study plan
Comparator: naproxen tablet 500 mg
DrugPrimary outcomes
-
Tender joint count
-
swollen joint count
-
patient's global assessment of disease activity
-
investigator's global assessment of disease activity
Secondary outcomes
-
Patient pain assessment
-
patient's global assessment of response to therapy
-
investigator's global assessment of response to therapy
Sponsors and collaborators
Lead sponsor
Merck Sharp & Dohme LLC
Industry
Registry information
Official study title
A Multicenter, Randomized, Parallel-Group, 8-Week, Double-Blind, and Active Comparator-Controlled Study to Assess the Efficacy, Safety, and Tolerability of Rofecoxib Tablet 25 mg Once Daily Versus Naproxen Table 500 mg Twice Daily in the Treatment of Chinese Patient With Rheumatoid Arthritis
Important dates
- Study start
- 2004
- Primary completion
- 2004
- Study completion
- 2004
- First posted
- Sep 12, 2005
- Registry last updated
- May 25, 2017
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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