Trial · NCT07892755
Liquid Biopsy-Based Early Screening for Endometrial Cancer in Regional Chinese Populations
NCT07892755, Recruiting, Guizhou Provincial People's Hospital
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Liquid Biopsy-Based Early Screening for Endometrial Cancer in Regional Chinese Populations. Trials, record NCT07892755. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07892755
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Liquid Biopsy-Based Early Screening for Endometrial Cancer in Regional Chinese Populations
- NCT number
- NCT07892755
- Status
- Recruiting
- Enrollment
- 512 participants, estimated
- Lead sponsor
- Guizhou Provincial People's Hospital
- Conditions
- Endometrial Cancer, Atypical Endometrial Hyperplasia
- First posted
- 2026-10-23
- Last updated
- 2026-10-23
Source ClinicalTrials.gov
Registered outcomes2
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Diagnostic performance (sensitivity and specificity) of the cfDNA fragmentomics model for early screening of endometrial cancer | At baseline (time of blood collection) | Evaluate the accuracy and specificity of a multi-omics cfDNA-based model (incorporating fragmentomics and copy number variation features) in predicting the risk of endometrial cancer. |
| Secondary | Ability of the cfDNA model to differentiate between benign and malignant endometrial lesions | At baseline (time of blood collection) | Evaluate the performance of the cfDNA-based model in distinguishing atypical endometrial hyperplasia (precancerous/benign) from endometrial cancer (malignant). |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers3
The papers the trial lists on ClinicalTrials.gov.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07892755
GET https://conductscience.org/api/trials/v1/NCT07892755/registered