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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03740672
Other study ID # GO-CINV
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date November 22, 2018
Est. completion date December 1, 2019

Study information

Verified date November 2018
Source Peking Union Medical College Hospital
Contact Lei Li, M.D.
Phone 8613911988831
Email lileigh@163.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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/).


Recruitment information / eligibility

Status Recruiting
Enrollment 1000
Est. completion date December 1, 2019
Est. primary completion date December 1, 2019
Accepts healthy volunteers
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Good performance status

- Aged 18 years or older

- Signed an approved informed consents

Exclusion Criteria:

- Not meeting all of the inclusion criteria

Study Design


Locations

Country Name City State
China Lei Li Beijing Beijing

Sponsors (1)

Lead Sponsor Collaborator
Lei Li

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary risk of chemotherapy induced nausea and vomiting The 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. One year
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