drugset / Trial / NCT03557424

BEFORE Study, Efficacy of Refigura

NCT03557424 ↗

Phase 4 Completed 165 enrolled Heilpflanzenwohl AG
RandomizedParallel-groupTriple-blindTreatment

Summary

The BEFORE study ((B) EFficacy Of REfigura) is designed to demonstrate the efficacy of REFIGURA®. It is a double-blind, randomized, monocentric study.

Timeline

Start
2017-04-26
Primary completion
2018-04-16
Completion
2018-04-16

Drugs

EvaluationDrugModalityDoseRoute
Subject KONJAC MANNAN Other / unclassified 1 g Oral
Subject KONJAC MANNAN Other / unclassified 1.34 g Oral
Subject Polyglucosamine Other / unclassified 0.5 g Oral
Subject Polyglucosamine Other / unclassified 1 g Oral

Indications

No indication recorded.