NCT Number: NCT00092703
Investigational Drug Versus an Approved Drug in Patients With Osteoarthritis (0663-061)(COMPLETED)
The purpose of this study is to compare the gastrointestinal tolerability of an investigational drug to an approved drug in the treatment of osteoarthritis during one year treatment period.
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Notify MeKey information
Age range
50 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 3
About this study
The duration of treatment is 12 months.
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Osteoarthritis of the knee, hip, hand or spine which requires the use of medications for pain relief
Exclusion criteria
- Known allergies to the study drugs
Treatment and study plan
Comparator: Diclofenac sodium
DrugPrimary outcomes
-
Discontinuations due to clinical and laboratory gastrointestinal adverse experiences during a 1 year treatment period.
Sponsors and collaborators
Lead sponsor
Organon and Co
Industry
Registry information
Official study title
A Randomized, Double-Blind, Multicenter Study to Evaluate the Tolerability and Effectiveness of Etoricoxib 90 mg q.d. vs. Diclofenac Sodium 50 mg t.i.d. in Patients With Osteoarthritis
Important dates
- Study start
- 2002
- Primary completion
- 2003
- Study completion
- 2003
- First posted
- Sep 28, 2004
- Registry last updated
- Aug 15, 2024
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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