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The objective of this study was to evaluate the various parameters involved in the occurrence of nausea / vomiting during the first cycle of chemotherapy for solid tumors or hematologic among a group of chemotherapy-naive patients, despite anti standardized-emetics protocols.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Centre de la Baie
Avranches, France
Centre hospitalier
Bayeux, France
Centre Maurice Tubiana
Caen, France
Centre François Baclesse
Caen, France
Centre hospitalier public du cotentin
Cherbourg-Octeville, France
Centre Jacques Monod
Flers, France
Start Date
July 1, 2011
Primary Completion Date
January 1, 2013
Completion Date
February 1, 2013
Last Updated
December 17, 2025
300
ACTUAL participants
Lead Sponsor
Centre Francois Baclesse
NCT06066138
NCT05702398
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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