Clinical trial · Observational
Observational, Bivariate Analysis of Clinical Big Data in Patients With Cervical Cancer
The First Affiliated Hospital of USTC (Anhui Provincial Hospital)
NCT06480617CI-TRIAL-00078385active not recruitingClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This is a large non-interventional observational bidirectional study planned to collect clinically relevant data and prognostic follow-up information of patients with cervical cancer who were seen at our center from 2010.01.01 to the end of this study.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Overall Survival Was Defined as Time From Surgery to Death From Any Cause or Last Follow-up | — | UNRESOLVED | — |
| Progression-free Survival Was Defined From Date of Surgery to Disease Progression Post-surgery or Death or Last Follow-up | — | UNRESOLVED | — |
Interventions
Interventions (0)
Data not yet available
No intervention recorded.
Design
Arms and outcomes
Arms (2)
- label
- LNM(+)
- description
- Postoperative pathology suggests lymph node metastasis
- label
- LNM(-)
- description
- Postoperative pathology did not suggest lymph node metastasis
Primary outcomes (1)
- measure
- progression-free survival
- timeFrame
- 5 years
Secondary outcomes (1)
- measure
- overall survival
- timeFrame
- 5 years
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. Age ≥ 18 years; 2. patients with a clear pathological diagnosis of cervical cancer; 3. all patients included in this study were diagnosed after 1 January 2010 4. Diagnosis or treatment of cervical cancer at the centres covered by this study; 5. exemption from informed consent or signing of an informed consent form. Exclusion Criteria: 1. Loss of contact during the follow-up period for no apparent reason; 2. Discharged from the hospital for follow-up treatment at an outside institution with unknown treatment status; 3. The investigator considers the patient unsuitable for participation in this study; 4. cases where the clinical diagnosis is in doubt or unclear.
References
Publications (0)
Data not yet available
No reference posted for this study.