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Clinical Trial Summary

This multi-center longitudinal study aims to compare the survival outcomes (including overall survival, progression-free survival and disease-free survival between uterine cervical patients receiving different surgical routes (vaginal, laparotomy and laparoscopy), which is the primary study objective. All clinical and pathological data would be retracted from case reviews, and all survival data would be reached by clinic, telephone and mail follow-up. This study also would analyze the impact on survival outcomes of other factors, including nerve-sparing techniques, neoadjuvant chemotherapy, neoadjuvant radiotherapy and infection of human papillomavirus. The predictive effects of different following protocol and imaging plans will be also compared. Last, the influences of surgical routes on the fertility outcomes (pregnancy and its complications) and the ovarian reserve are important secondary study objectives.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03738969
Study type Observational
Source Peking Union Medical College Hospital
Contact Lei Li, M.D.
Phone 13911988831
Email lileigh@163.com
Status Recruiting
Phase
Start date November 10, 2018
Completion date December 23, 2023

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