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Clinical Trial Summary

This study aims to estimate the effect of the practice of a short-term partial fasting compared to a usual alimentation on nausea and vomiting within 5 days after the start of a chemotherapy session on 2 successive chemotherapy courses (4 sessions of chemotherapy) in patients starting treatment with highly emetogenic chemotherapy (ABVD or AVD protocol).


Clinical Trial Description

Patients in fasting arm will practice partial fasting during 3 days (D-1, D1 (D day of chemotherapy) and D2) following a food guide during 4 chemotherapy sessions. Patients in usual alimentation arm will continue to take food as usual practice. In each arm, patients will be interviewed at each chemotherapy sessions about nausea and vomiting (number and intensity of nausea and vomiting, treatments taken). Denutrition, quality of life improvement, compliance to partial fasting, treatment response will be evaluate too. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04141514
Study type Interventional
Source Centre Hospitalier Universitaire de la Réunion
Contact Mélanie BEGORRE
Phone +262 (0)262 90 78 85
Email melanie.begorre@chu-reunion.fr
Status Recruiting
Phase N/A
Start date January 20, 2022
Completion date June 19, 2025

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