drugset / Trial / NCT03182179

Efficacy of Ondansetron in LARS Treatment

NCT03182179

RandomizedCrossoverQuadruple-blindTreatment

Summary

Patients will be randomized (1:1 ratio) to receive either 4 weeks of Ondansetron followed by 4 weeks of placebo (O-P sequence) or 4 weeks of placebo followed by 4 weeks of Ondansetron (P-O sequence). It will be one week of washout between the two treatments. During the treatment questionnaires will be completed by the patients to evaluate the efficacy of the study treatment and the quality of live.

Timeline

Start
2016-11-01
Primary completion
2021-11-19
Completion
2021-11-19

Drugs

EvaluationDrugModalityDoseRoute
Subject Ondansetron Other / unclassified 4 mg Oral

Indications