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EudraCT Number: 2004-001069-17 Sponsor Protocol Number: CSPI135ZDE04 Start Date: 2004-09-16
Sponsor Name: Novartis Pharma GmbH
Full Title: A double-blind, active-controlled, randomized, multicenter, parallel-group 2 day comparison of 1000 mg propyphenazone / 80 mg codeine (applied as two suppositories) combination therapy versus a 100...
Medical condition: acute, at least moderate to severe biliary or urogenital pain
Disease: Version SOC Term Classification Code Term Level
7.0 10004670 low
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: LT (Completed)
Trial results: View results
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