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Management of Nausea and Vomiting Chemotherapy-induced in Normandy

Completed
Conditions
Cancer
Nausea
Vomiting
Registration Number
NCT01440465
Lead Sponsor
Centre Francois Baclesse
Brief Summary

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.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
300
Inclusion Criteria
  • Aged over 18 years
  • 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

This does not concern patients who:

  • 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.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
acute nausea and vomiting2 years

acute nausea and vomiting and / or delayed measured by the tool of anti emetic MAT MASCC.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (6)

Centre de la Baie

πŸ‡«πŸ‡·

Avranches, France

Centre hospitalier

πŸ‡«πŸ‡·

Bayeux, France

Centre FranΓ§ois Baclesse

πŸ‡«πŸ‡·

Caen, France

Centre Jacques Monod

πŸ‡«πŸ‡·

Flers, France

Centre Maurice Tubiana

πŸ‡«πŸ‡·

Caen, France

Centre hospitalier public du cotentin

πŸ‡«πŸ‡·

Cherbourg-Octeville, France

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