NCT03291236UnknownNot Applicable
Survival Outcomes of Uterine Cervical Malignancies in Chinese Population
Lei Li1 site in 1 country5,000 target enrollmentStarted: January 1, 2017Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Sponsor
- Enrollment
- 5,000
- Locations
- 1
- Primary Endpoint
- Overall survival
Study Overview
Brief Summary
This study aims to determine survival outcomes (overall survival and progression-free survival) of primary malignancies of uterine cervix in China and relevant risk factors in a prospective cohort study.
Study Design
- Study Type
- Observational
- Observational Model
- Cohort
- Time Perspective
- Prospective
Eligibility Criteria
- Sex
- Female
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Primary malignancies of uterine cervix.
Exclusion Criteria
- •Secondary malignancies of uternie cervix.
Outcomes
Primary Outcomes
Overall survival
Time Frame: 5 years
Duration from diagnosis to recurrence
Progression-free survival
Time Frame: 5 years
Duration from last treatment after remission to recurrence
Secondary Outcomes
No secondary outcomes reported
Investigators
Lei Li
Professor
Peking Union Medical College Hospital
Study Sites (1)
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