Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT03239821Completed
Randomised, double-blind trial (4 arms), sponsored by UZ Leuven. Primary endpoints: Incidence, frequency, severity, seriousness and relatedness of Adverse Events at 8 hours, Success rate in completing the procedure (placement and removal VIPUN Balloon Catheter) at 8 hours and 1 more. Started Sep 2017; status: completed.
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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