Clinical trial · Observational
Cervical Cytology DNA Methylation for Endometrial Lesion Screening and Follow-up
A Multicenter Study on Cervical Cytology DNA Methylation for Screening and Follow-up of Endometrial Lesions
- 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)
The goal of this observational study is to evaluate the accuracy of a novel molecular test for screening and monitoring endometrial lesions in women at medium-to-high risk for endometrial cancer. The main questions it aims to answer are: * What is the sensitivity and specificity of the CISENDO test (a DNA methylation test on cervical cytology samples) for detecting histologically confirmed endometrial intraepithelial neoplasia (EIN) or invasive endometrial cancer? * How do DNA methylation levels change during the follow-up of endometrial lesions? Researchers will compare the results of the CISENDO test to the results from the standard diagnostic procedure (hysteroscopy with histology) to see if the molecular test can reliably identify high-risk lesions and track disease progression. Participants will: * Provide a residual liquid-based cervical cytology sample for the CISENDO test. * Undergo a standard diagnostic hysteroscopy examination (with or without biopsy) for comparison. * Some participants will return for follow-up visits at 6 and 12 months for repeat methylation testing and/or hysteroscopy to monitor their condition.
Conditions
Conditions (5)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Cervical Smears | — | UNRESOLVED | — |
| DNA Methylation | — | UNRESOLVED | — |
| Early Detection of Cancer | — | UNRESOLVED | — |
| Endometrial Hyperplasia | — | UNRESOLVED | — |
| Endometrial Neoplasms | Endometrial Neoplasm | ONTOLOGY_EXACT | 0.98 |
Interventions
Interventions (0)
Data not yet available
Design
Arms and outcomes
Arms (1)
- label
- Endometrial Cancer Risk Cohort
- description
- This is a prospective, observational cohort of women at medium-to-high risk for endometrial cancer. All participants undergo baseline cervical cytology sampling for DNA methylation testing (CISENDO) and diagnostic hysteroscopy. Follow-up strategy is stratified based on initial methylation results and risk factors, with some receiving repeat methylation testing and/or hysteroscopy at 6 and 12 months, and others receiving methylation testing only.
Primary outcomes (1)
- measure
- Sensitivity of CISENDO Test
- timeFrame
- Baseline (at the time of initial hysteroscopy)
- description
- The proportion of participants with histologically confirmed endometrial intraepithelial neoplasia (EIN) or invasive endometrial cancer who have a positive CISENDO test result at baseline.
Secondary outcomes (5)
- measure
- Dynamic Change in DNA Methylation Level
- timeFrame
- From baseline to 12 months
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. Participants must be 18 years of age or older. 2. Participants must possess medium-to-high risk factors for endometrial cancer as defined by Chinese consensus guidelines and are scheduled for hysteroscopic evaluation; OR are currently undergoing conservative treatment (e.g., progesterone therapy or endometrial ablation) for endometrial lesions, and have not received chemotherapy. 3. Participants must be capable and willing to provide written informed consent. 4. Participants must be willing to undergo at least one follow-up assessment within 1 year. 5. Participants must have an intact cervix (a history of LEEP or conization is acceptable). Exclusion Criteria: 1. Current treatment for any gynecologic malignancy other than endometrial cancer. 2. Current or untreated cervical, vaginal, or vulvar intraepithelial neoplasia or carcinoma. 3. History of total or subtotal hysterectomy, trachelectomy, radical trachelectomy, or pelvic radiotherapy. 4. Active lower genital tract bleeding. 5. Immunosuppressed state (e.g., HIV infection, status post organ transplantation). 6. Failure to undergo the planned hysteroscopic evaluation and follow-up within 1 year after the initial assessment. 7. Failed hysteroscopic procedure. 8. Any other condition that, in the opinion of the investigator, makes the participant unsuitable for inclusion in the study.
References
Publications (0)
Data not yet available