NCT Number: NCT00142558
A Study Evaluating the Effect of Etoricoxib and Indomethacin in the Treatment of Acute Gout (0663-081)(COMPLETED)
A study to evaluate the effects of etoricoxib and indomethacin in the treatment of acute gout.
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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
- Males or females at least 18 years of age who have acute gout.
Treatment and study plan
Comparator: indomethacin 75 mg sustained release capsule / Duration of Treatment: 5 Days
DrugPrimary outcomes
-
Patient assessment of pain (0- to 4- Likert scale)
Secondary outcomes
-
Patient Global Assessment of Response to Therapy (0- to 4- point scale)
-
Investigator Global Assessment of Response to Therapy (0- to 4- point scale)
-
Tenderness of the study joint (0- to 3-point scale)
-
Swelling of the study joint (0- to 3-point scale)
Sponsors and collaborators
Lead sponsor
Organon and Co
Industry
Registry information
Official study title
A Randomized, Double-Blind, Active-Comparator-Controlled 5-Day Trial of the Effect of Etoricoxib 120 mg Versus Indomethacin 150 mg in the Treatment of Acute Gout
Important dates
- Study start
- 2005
- Primary completion
- 2005
- Study completion
- 2005
- First posted
- Sep 2, 2005
- 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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