Clinical Trials Directory

Trials / Completed

CompletedNCT04342780

Prevalence of Delayed Chemotherapy Associated Nausea

Delayed Chemotherapy-induced Nausea: A Multi-center Prevalence Survey in Adult Oncology Patients in Clinical Practice

Status
Completed
Phase
Study type
Observational
Enrollment
172 (actual)
Sponsor
Antje Koller · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study evaluates the prevalence of delayed chemotherapy induced nausea in adult oncology patients in real clinical practice of day clinics.

Detailed description

Chemotherapies are rated to have a high to minimal emetogenic potential in oncology patients. Their potential to induce delayed nausea is supposed to often be higher than their emetogenic potential. However, data on delayed chemotherapy-related nausea are scarce, which is problematic because nausea (a) has a large impact on patients quality of life and treatment decisions, (b) is often underestimated by health care professionals, (c) is less responsive to commonly used antiemetic medication, and (d) may even be different from rates that have been established in controlled clinical trials. Therefore, the aim of this study is to assess the prevalence of delayed chemotherappy-induced nausea in adult oncology patients in dayclinics.

Conditions

Timeline

Start date
2020-06-29
Primary completion
2022-05-31
Completion
2022-05-31
First posted
2020-04-13
Last updated
2024-04-19

Locations

1 site across 1 country: Switzerland

Source: ClinicalTrials.gov record NCT04342780. Inclusion in this directory is not an endorsement.