System to Evaluate the Risk of Lymph Node Metastasis Preoperatively in Cervical Cancer
NCT ID: NCT06032481
Last Updated: 2023-09-13
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
426 participants
OBSERVATIONAL
2012-01-01
2023-03-15
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Prediction of Cervical Lymph Node Metastasis in Papillary Thyroid Carcinoma Based on Ultrasound and Cytological Images
NCT06399159
Prospective Study on the Clinical Prognosis of Bilateral Central Lymph Node Dissection in the Patients With Unilateral Thyroid Papillary Carcinoma
NCT02648399
Bilateral Elective Neck Dissection in Salvage Total Laryngectomy
NCT05746780
Central Cervical Dissection for Clinical Node Negative Papillary Thyroid Carcinoma
NCT03813173
Identification of Surgical Management of Lymph Node Basins and Surgical Practice Patterns Among Sarcoma Surgeons
NCT04553744
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
RETROSPECTIVE
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
surgery
Patients confirmed cervical cancer were undergone radical hysterectomy with pelvic lymphadenectomy
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* FIGO stage IB1-IIA1
* Undergone radical hysterectomy with pelvic lymphadenectomy
* Peformed pelvic MRI examination preoperatively
Exclusion Criteria
* Underwent neoadjuvant radiotherapy preoperatively
* Underwent neoadjuvant chemotherapy preoperatively
* Incomplete or inaccuratemedical records
25 Years
70 Years
FEMALE
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Fujian Maternity and Child Health Hospital
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Yebin Feng
Director
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Pengming Sun, Ph.D
Role: PRINCIPAL_INVESTIGATOR
Fujian Maternity and Child Health Hospital
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
FujianMCHH-Xu01
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.