Skip to main content
Clinical Trials/NCT05634798
NCT05634798
Unknown
Not Applicable

An Observational Study Based on Endometrial Cancer Risk Screening Model

Peking Union Medical College Hospital1 site in 1 country2,000 target enrollmentDecember 1, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Endometrial Neoplasms
Sponsor
Peking Union Medical College Hospital
Enrollment
2000
Locations
1
Primary Endpoint
No endometrial cancer or precancerous lesions
Last Updated
3 years ago

Overview

Brief Summary

The goal of this observational study is to test the efficiency of our endometrial cancer risk screening calculator, and improve the endometrial cancer risk screening model to form a stable and reliable non-invasive auxiliary diagnostic tool with high sensitivity and specificity in healthy women.The main question it aims to answer is:

·the efficiency of our endometrial cancer risk screening calculator Participants will be collected demographic information, as well as ultrasound, blood routine test and other test results, which will be entered into the endometrial cancer risk screening calculator to obtain high-risk or low-risk prediction results.

Registry
clinicaltrials.gov
Start Date
December 1, 2022
End Date
December 1, 2023
Last Updated
3 years ago
Study Type
Observational
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Age: 18-70;
  • The annual update of questionnaire information required by the calculator can be completed, and the gynecological examination, gynecological B-ultrasound and blood test can be evaluated once a year, and the follow-up can be at least 1 year; The patient or family members can understand the research scheme and are willing to participate in the study, and provide e-book informed consent.

Exclusion Criteria

  • Endometrial cancer or precancerous lesions have been diagnosed;
  • Previous or current malignant tumor, currently receiving radiotherapy and chemotherapy, endocrine, targeted and immunotherapy;
  • History of endometrial resection or total hysterectomy;
  • Pregnant or lactating women;
  • The patient or family member could not understand the conditions and objectives of this study.

Outcomes

Primary Outcomes

No endometrial cancer or precancerous lesions

Time Frame: 1 year

The study object did not show B-ultrasound and clinical symptoms which indicate endometrial cancer or precancerous lesions.

Obtained endometrial pathological specimens due to any factors

Time Frame: 1 year

The study object was obtained endometrial pathological specimen within one year due to any factor.

Study Sites (1)

Loading locations...

Similar Trials