Skip to content

Longitudinal Study of Different Surgical Approaches in Chinese Patients of Uterine Cervical Cancer

Longitudinal Study of Different Surgical Approaches in Chinese Patients of Cervical Cancer

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03738969
Enrollment
3000
Registered
2018-11-13
Start date
2018-11-10
Completion date
2023-12-23
Last updated
2018-11-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Laparoscopy, Laparotomy, Mortality, Recurrence, Survival, Uterine Cervical Neoplasms

Brief 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.

Interventions

Radical hysterectomy applied by laparotomy

Radical hysterectomy applied by laparoscopic

Sponsors

Lei Li
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
No

Inclusion criteria

* Pathological confirmed as uterine cervical cancer * Having definite clinical information * Having received radical hysterectomy or trachelectomy

Exclusion criteria

* Not satisfying any of the inclusion criteria

Design outcomes

Primary

MeasureTime frameDescription
Progression-free survivalFive yearsLength of time during and after the treatment of cervical cancer, that a patient lives with the disease but it does not get worse

Secondary

MeasureTime frameDescription
Overall survivalFive yearsThe length of time from either the date of diagnosis or the start of treatment for a disease, such as cancer, that patients diagnosed with the disease are still alive. In a clinical trial, measuring the overall survival is one way to see how well a new treatment works.
Disease-free survivalFive yearsIn cancer, the length of time after primary treatment for a cancer ends that the patient survives without any signs or symptoms of that cancer. In a clinical trial, measuring the disease-free survival is one way to see how well a new treatment works.

Other

MeasureTime frameDescription
Pregnancy rateFive yearsProportion of patients who have been pregnant after the fertility-preserving radical trachelectomy

Countries

China

Contacts

Primary ContactLei Li, M.D.
lileigh@163.com13911988831

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 2, 2026