Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT02812199Unknown
Randomised, open-label trial (3 arms), sponsored by STS Medical Group. Primary endpoint: Composite Removable Sinus Stent efficacy compared to standard of care at 12 weeks. Status: unknown.
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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