LEMON trial
Ontology highlight
ABSTRACT: Interventions: Oral ingestion of test tablets with L.E.M. or placebo (12 grains per a day; 12 weeks)
Primary outcome(s): Evaluate the change in CIPN VAS (numbness) from start to the end of the initial treatment period (weeks 0-12) in the placebo and low-dose groups
Study Design: randomized controlled trial, double blind, placebo control, parallel assignment, treatment purpose
DISEASE(S): Chemotherapy-induced Peripheral Neuropathy,Cipn
PROVIDER: 2615440 | ecrin-mdr-crc |
REPOSITORIES: ECRIN MDR
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