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Adherence to the Antiemesis National Comprehensive Cancer Network (NCCN) Guideline

Adherence to the Antiemesis National Comprehensive Cancer Network (NCCN) Guideline in Chinese Patients of Gynecologic Malignancies

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03740672
Enrollment
1000
Registered
2018-11-14
Start date
2018-11-22
Completion date
2019-12-01
Last updated
2018-11-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chemotherapy-induced Nausea and Vomiting, Gynecologic Cancer

Brief summary

This study aims to investigate the adherence to the antiemesis NCCN guideline in Chinese patients of gynecologic malignancies, who are given chemotherapy treatment. The risk of chemotherapy induced nausea and vomiting (CINV) is calculated by the questionnaire supported by the website CINV Risk Assessment (http://www.riskcinv.org/).

Interventions

None listed

Sponsors

Lei Li
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum

Inclusion criteria

* Good performance status * Aged 18 years or older * Signed an approved informed consents

Exclusion criteria

* Not meeting all of the inclusion criteria

Design outcomes

Primary

MeasureTime frameDescription
risk of chemotherapy induced nausea and vomitingOne yearThe risk of chemotherapy induced nausea and vomiting is calculated by the questionnaire supported by the website CINV Risk Assessment (http://www.riskcinv.org/). The difference of patients adhered to and not to NCCN guideline is compared.

Countries

China

Contacts

Primary ContactLei Li, M.D.
lileigh@163.com8613911988831

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026