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Clinical Trials/NCT03291236
NCT03291236
Unknown
Not Applicable

Survival Outcomes of Uterine Cervical Malignancies in Chinese Population

Lei Li1 site in 1 country5,000 target enrollmentJanuary 1, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Uterine Cervical Neoplasms
Sponsor
Lei Li
Enrollment
5000
Locations
1
Primary Endpoint
Overall survival
Last Updated
8 years ago

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.

Registry
clinicaltrials.gov
Start Date
January 1, 2017
End Date
January 1, 2023
Last Updated
8 years ago
Study Type
Observational
Sex
Female

Investigators

Sponsor
Lei Li
Responsible Party
Sponsor Investigator
Principal Investigator

Lei Li

Professor

Peking Union Medical College Hospital

Eligibility Criteria

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

Study Sites (1)

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