Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT02462837Phase 2Terminated
Phase 2, randomised, double-blind trial of mirabegron in ureteral stent-related symptoms (USRS) (2 arms), sponsored by Southern Illinois University. Primary endpoints: Incontinence Symptom Severity Index at 2 weeks, Number of Micturitions Per 24 Hours at 2 weeks and 1 more. Started May 2015; status: terminated.
Beyond the preview
Study design, results and competitive context are available in the Gosset platform where reported.
Available in the Gosset platform where reported.
Available in the Gosset platform where reported.
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