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NCT03291275 Clinical Trial

Survival Outcomes of Uterine Malignancies in Chinese Population

Endometrial Neoplasms Clinical Trial

Official title:
Survival Outcomes of Uterine Malignancies in Chinese Population

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT03291275
Other study ID # SOUM-1
Secondary ID
Status Recruiting
Phase N/A
First received September 20, 2017
Last updated February 7, 2018
Start date September 1, 2017
Est. completion date September 1, 2023

Study information
Verified date February 2018
Source Peking Union Medical College Hospital
Contact Lei Li, MD
Phone 13911988831
Email lileigh@163.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study aims to determine survival outcomes (overall survival and progression-free survival) of primary uterine malignancies in China and relevant risk factors in a prospective cohort study.

Recruitment information / eligibility
Status Recruiting
Enrollment 10000
Est. completion date September 1, 2023
Est. primary completion date September 1, 2022
Accepts healthy volunteers No
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria:

- Primary uterine malignancies.

Exclusion Criteria:

- Metastatic malignancies to uterine corpus

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Follow-up for death and recurrence
All patients are followed up to determine definite date of diagnosis, recurrence and death.

Locations
Country Name City State
China Lei Li Beijing China/Beiing

Sponsors (1)
Lead Sponsor Collaborator
Lei Li

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary Overall survival Survival duration from diagnosis to death 5 years
Primary Progression-free survival Survival duration from last treatment after remission to recurrence 5 years
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