Prevalence of Delayed Chemotherapy Associated Nausea

NCT ID: NCT04342780

Last Updated: 2024-04-19

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

172 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-06-29

Study Completion Date

2022-05-31

Brief Summary

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

Detailed Description

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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

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Chemotherapy-induced Nausea and Vomiting

Study Design

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Observational Model Type

COHORT

Study Time Perspective

CROSS_SECTIONAL

Eligibility Criteria

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Inclusion Criteria

* first day of chemotherapy of a new cycle (any cycle)
* speak and write German
* sign the consent forms

Exclusion Criteria

* cognitive or linguistic impairments that would significantly impede consent or participation (as assessed by the nurses in charge)
* accompanying radiotherapy;
* pre-existing nausea within three days before the start of the first chemotherapy in this cycle; and
* prior participation in CINrate (each person participates only once)
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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ZETUP St. Gallen

UNKNOWN

Sponsor Role collaborator

Dr.-Hans-Altschüler-Stiftung

UNKNOWN

Sponsor Role collaborator

University Medical Center Freiburg

OTHER

Sponsor Role collaborator

Spital Thurgau AG

OTHER

Sponsor Role collaborator

Antje Koller

OTHER

Sponsor Role lead

Responsible Party

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Antje Koller

Principal Investigator

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

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Antje Koller

Role: PRINCIPAL_INVESTIGATOR

Ostschweizer Fachhochschule St. Gallen

Locations

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ZeTuP

Sankt Gallen, , Switzerland

Site Status

Countries

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Switzerland

Other Identifiers

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CINrate

Identifier Type: -

Identifier Source: org_study_id

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