Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT04150380Phase 2Completed
Phase 2, randomised, double-blind trial of Lactobacillus rhamnosus GG in post-traumatic stress disorder (PTSD) and functional bowel disorder (FBD) (2 arms), sponsored by VA Eastern Colorado Health Care System. Primary endpoint: Plasma concentration of C-reactive protein at 8 weeks. Started Aug 2020; 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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