A Multi-centre, Phase II, Double-blind, Randomised, Placebo-controlled, Parallel Group, Dose-ranging Study in Patients With Faecal Incontinence; to Evaluate the Efficacy, Safety and Tolerability of Locally Applied NRL001 Over an 8 Week Treatment Period

Clinical Trial ID NCT01656720

PubWeight™ 0.75‹?›

🔗 Visit the ClinicalTrials.gov page for NCT01656720

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Libertas: a phase II placebo-controlled study of NRL001 in patients with faecal incontinence showed an unexpected and sustained placebo response. Int J Colorectal Dis 2016 0.75
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