Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT02918487Unknown
Randomised, double-blind trial (2 arms), sponsored by Composite Interceptive Med-Science Laboratories. Primary endpoints: Number of patients with 15% increase in forced expiratory volume (FEV1) from baseline at 6 months and Number of patients with 50 L/min peak expiratory flow rate (PEFR) from baseline at 6 months. 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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