Atlas Trials

Study of Non Inferiority Bi-Profenid® 200mg Versus Bi-Profenid® 300mg Among Patients Presenting of the Post-traumatic or Rheumatologic Acute Affections of the Locomotor Apparatus (BIPROPAIN)

Clinical trial NCT00810121 · COMPLETED

Trial details

NCT number
NCT00810121
Sponsor
Sanofi
Status
COMPLETED
Phase
Phase 3
Study type
INTERVENTIONAL
Pain
Start date
2008-11-01
Primary completion
2009-06-01
Enrollment
409

View on ClinicalTrials.gov

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