Management of Nausea and Vomiting Chemotherapy-induced in Normandy
NCT ID: NCT01440465
Last Updated: 2025-12-17
Study Results
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View full resultsBasic Information
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COMPLETED
300 participants
OBSERVATIONAL
2011-07-31
2013-02-28
Brief Summary
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Detailed Description
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Conditions
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Study Design
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OTHER
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* With solid tumors or hematologic in first line chemotherapy, administered intravenously,
* Able to understand the meaning of the questions
* Having given their written consent to participate in the survey.
Exclusion Criteria
* Do not give their consent for participation
* Do not speak French
* Suffer from cognitive deficits
* Are under therapy
* Must receive a combination of radio-chemotherapy
* Present an occlusive syndrome
* Metastases (s) brain (s) clinically symptomatic (s) or radiologically proven (s) or a (of) tumor (s) brain (s)
* Have been previously treated with chemotherapy
* Present a cons-indication to corticosteroids, with anti-serotonin or NK1 receptor inhibitors
* Pregnant or breastfeeding.
18 Years
ALL
No
Sponsors
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Centre Francois Baclesse
OTHER
Responsible Party
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Principal Investigators
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JOLY Florence, Pr
Role: PRINCIPAL_INVESTIGATOR
Centre François Baclesse
Locations
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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
Countries
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Other Identifiers
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NAVI
Identifier Type: -
Identifier Source: org_study_id