The Clinical Significance of Sentinel Lymph Node Imaging Combined With Imaging Examination in Pelvic and Peritoneal Lymphadenectomy for Endometrial Carcinoma
Primary Purpose
Endometrial Carcinoma, Lymphadenectomy
Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Pelvic and Peritoneal Lymphadenectomy
Sponsored by
About this trial
This is an interventional treatment trial for Endometrial Carcinoma
Eligibility Criteria
Inclusion Criteria:
- Females who are diagnosed with endometrial carcinoma;
- Patients who are willing to receive primary non-reserved fertility function surgery to treat their disease;
- Patients who are agreed to participated in this prospective cohort study.
Exclusion Criteria:
- Patients who still have the will to have pregnancy;
- Patients who have other diseases or heavy injuries that will interfere with the results;
- Simultaneous participation in another clinical study with investigational medicinal product(s) or researcher thinks the subjects are not suitable for this trial.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
No Intervention
Experimental
Arm Label
Negative 1
Negative 2
Arm Description
Patients in this arm will not undergo Pelvic and Peritoneal Lymphadenectomy.
Patients in this arm will undergo Pelvic and Peritoneal Lymphadenectomy.
Outcomes
Primary Outcome Measures
the number (s) of pelvic and abdominal lymph node metastasis
the specific number of pelvic and abdominal lymph nodes that are invaded by metastatic endometrial carcinoma
the percentage (%) of pelvic and abdominal lymph node metastasis
the specific percentage of pelvic and abdominal lymph nodes that are invaded by metastatic endometrial carcinoma
the coincidence rate (%) of pelvic and abdominal lymph node imaging, sentinel lymph node imaging and pathological diagnosis
by performing chi-square test by SPSS 17.0,we plan to calculate the coincidence rate of three clinical examination
the effect of pelvic lymphadenectomy on the prognosis of endometrial carcinoma patients
by setting up the control group and experimental group and conducting follow-up,we are determined to know whether pelvic lymphadenectomy would influence the prognosis of endometrial carcinoma
Secondary Outcome Measures
Full Information
NCT ID
NCT03877627
First Posted
March 10, 2019
Last Updated
October 27, 2020
Sponsor
Second Affiliated Hospital of Wenzhou Medical University
1. Study Identification
Unique Protocol Identification Number
NCT03877627
Brief Title
The Clinical Significance of Sentinel Lymph Node Imaging Combined With Imaging Examination in Pelvic and Peritoneal Lymphadenectomy for Endometrial Carcinoma
Official Title
The Clinical Significance of Sentinel Lymph Node Imaging Combined With Imaging Examination in Pelvic and Peritoneal Lymphadenectomy for Endometrial Carcinoma
Study Type
Interventional
2. Study Status
Record Verification Date
October 2020
Overall Recruitment Status
Unknown status
Study Start Date
April 1, 2022 (Anticipated)
Primary Completion Date
March 15, 2023 (Anticipated)
Study Completion Date
April 1, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Second Affiliated Hospital of Wenzhou Medical University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
The aim of this prospective cohort study is to explore the clinical significance of sentinel lymph node imaging combined imaging examination evaluation in pelvic and peritoneal lymphadenectomy for endometrial carcinoma management.
Detailed Description
The clinical data including surgical procedure, the situation of sentinel lymph node imaging and pathological results of patients with endometrial carcinoma treated in our hospitals between April 2019 and April 2021 will be analyzed in this study to clarify the homogeneity of imaging evaluation, sentinel lymph node development evaluation and pathological results.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Endometrial Carcinoma, Lymphadenectomy
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
60 patients who were assessed negative by sentinel lymph node imaging combined with imaging were randomized to undergo pelvic and peritoneal lymphadenectomy.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Negative 1
Arm Type
No Intervention
Arm Description
Patients in this arm will not undergo Pelvic and Peritoneal Lymphadenectomy.
Arm Title
Negative 2
Arm Type
Experimental
Arm Description
Patients in this arm will undergo Pelvic and Peritoneal Lymphadenectomy.
Intervention Type
Procedure
Intervention Name(s)
Pelvic and Peritoneal Lymphadenectomy
Intervention Description
Patients in arm 2 will be randomized to undergo pelvic and peritoneal lymphadenectomy to treat their endometrial carcinoma.
Primary Outcome Measure Information:
Title
the number (s) of pelvic and abdominal lymph node metastasis
Description
the specific number of pelvic and abdominal lymph nodes that are invaded by metastatic endometrial carcinoma
Time Frame
1 year during the perioperative period
Title
the percentage (%) of pelvic and abdominal lymph node metastasis
Description
the specific percentage of pelvic and abdominal lymph nodes that are invaded by metastatic endometrial carcinoma
Time Frame
1 year during the perioperative period
Title
the coincidence rate (%) of pelvic and abdominal lymph node imaging, sentinel lymph node imaging and pathological diagnosis
Description
by performing chi-square test by SPSS 17.0,we plan to calculate the coincidence rate of three clinical examination
Time Frame
1 year during the perioperative period
Title
the effect of pelvic lymphadenectomy on the prognosis of endometrial carcinoma patients
Description
by setting up the control group and experimental group and conducting follow-up,we are determined to know whether pelvic lymphadenectomy would influence the prognosis of endometrial carcinoma
Time Frame
1 year during the perioperative period
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
10 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Females who are diagnosed with endometrial carcinoma;
Patients who are willing to receive primary non-reserved fertility function surgery to treat their disease;
Patients who are agreed to participated in this prospective cohort study.
Exclusion Criteria:
Patients who still have the will to have pregnancy;
Patients who have other diseases or heavy injuries that will interfere with the results;
Simultaneous participation in another clinical study with investigational medicinal product(s) or researcher thinks the subjects are not suitable for this trial.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yu ZHAO, Ph.D
Phone
13777760306
Email
zhaoyu196035@163.com
12. IPD Sharing Statement
Learn more about this trial
The Clinical Significance of Sentinel Lymph Node Imaging Combined With Imaging Examination in Pelvic and Peritoneal Lymphadenectomy for Endometrial Carcinoma
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