AzTrials
AzTrials

Uterine FibroidNCT07269535

A Prospective Validation Study of Radiomics in the Differential Diagnosis of Uterine Leiomyoma and Uterine Sarcoma

An observational study of Uterine Fibroid and Uterine Sarcoma, run by Tongji Hospital.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record

Search all trials

Trial summary

In our previous study, based on the multi-center clinical big data collected from January 2012 to January 2025, we have completed the construction of a multimodal early warning model for the malignant transformation of uterine fibroids. Read more about this study

Who is it for?
Any age, women only
How many people
500 participants
Where
No sites listed yet
Study dates
30 Sep 2026to 1 Jan 2050
How long will I take part?
5 Years
Phase
Observational

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • Women only
  • No healthy volunteers
  • Child, Adult, Older adult

Study population: Patients with a pathological diagnosis of uterine leiomyoma or uterine sarcoma will be recruited.

  1. Inclusion Criteria: 1.1 Patients clinically evaluated and radiologically examined (including MRI, particularly T2WI and DWI sequences) who are diagnosed with uterine leiomyoma or considered highly suspected of uterine sarcoma, in combination with preliminary pathological findings. 1.2 Patients scheduled for surgical treatment or those eligible for long-term standardized follow-up. 1.3 Patients who are able to understand the study procedures and voluntarily sign the written informed consent form.
  2. Exclusion Criteria:

2.1 Patients with severe organic diseases or a previous confirmed diagnosis of other malignant uterine tumors.

2.2 Patients unable to complete baseline examinations, unable to comply with long-term follow-up, or unwilling to provide written informed consent.

Trial locations and contacts

No sites are listed yet. Contact the study team or a site near you to ask about taking part.

About this study

In our previous study, based on the multi-center clinical big data collected from January 2012 to January 2025, we have completed the construction of a multimodal early warning model for the malignant transformation of uterine fibroids. The model was mainly based on T2WI and DWI sequences, and was trained and optimized by support vector machine (SVM) algorithm. In the retrospective study and internal validation, the model shows high sensitivity and specificity, which preliminarily proves that it has good application potential in identifying high-risk groups and predicting the risk of malignant transformation of uterine fibroids.

However, there are still some limitations in retrospective studies and internal validation results, and its application value, universality and stability in real clinical environment have not been fully verified. Therefore, we plan to conduct a prospective validation study in consecutive patients enrolled after January 2025 to evaluate the clinical performance and generalization of the model in predicting the malignant tendency or risk of malignant transformation of uterine fibroids through practical application in the real population, and further analyze the operability in the actual diagnosis and treatment process and the potential value for patient management. This study will provide reliable evidence for early screening, follow-up management and individualized treatment of high-risk population, and has important clinical and public health significance for improving the early diagnosis rate, reducing the risk of malignant transformation and improving the prognosis of patients with uterine fibroids.

Read the detailed description

Uterine fibroids are the most common benign gynecological tumors among women of reproductive age in China, with a prevalence of 20-30% among women over 30 years old and a trend toward younger onset. Despite advances in minimally invasive techniques and pharmacological therapies during the "12th Five-Year Plan," the incidence of uterine fibroids continues to rise due to rapid socioeconomic development, environmental changes, lifestyle shifts, and delayed childbearing. As a result, uterine fibroids have become a major public health concern. Understanding the mechanisms underlying the onset, recurrence, and malignant transformation of fibroids, developing fertility-preserving individualized treatment strategies, and identifying high-risk populations remain key challenges in reproductive and women's health research.

To address these challenges, our multicenter collaborative group, led by Tongji Hospital and supported by the National Clinical Research Center for Obstetrics and Gynecology, has established a large-scale systematic database integrating clinical, imaging, pathological, laboratory, and molecular data from multiple tertiary hospitals. Based on multicenter clinical big data collected from January 2012 to January 2025, we have developed a multimodal early-warning model for the malignant transformation of uterine fibroids. This model, primarily incorporating T2WI and DWI features and optimized using a support vector machine (SVM) algorithm, demonstrated high sensitivity and specificity in retrospective analysis and internal validation, suggesting promising potential for identifying high-risk individuals.

However, retrospective designs inherently limit the assessment of the model's real-world clinical applicability, generalizability, and stability. Therefore, beginning in January 2025, we plan to conduct a prospective validation study in consecutively enrolled patients to evaluate the model's diagnostic performance in routine clinical practice, its feasibility in real-world diagnostic workflows, and its potential value for early screening, follow-up management, and individualized treatment of high-risk populations. This study is expected to provide robust evidence to improve early detection, reduce malignant transformation risk, and ultimately enhance clinical outcomes and public health impact.

Being tested
No intervention (observational study)
Keywords
prospective observational study, Uterine Fibroid, uterine sarcoma, AI (Artificial Intelligence), Radiomic, MRI
Medical subject headings
Leiomyoma

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • No intervention (observational study)Other

    This study is a retrospective observational study without intervention.

Study groups in NCT07269535
Study groupRoleWhat they receive
Patients with a pathological diagnosis of uterine fibroidsNot described
Receives: Other: No intervention (observational study)
Patients with a pathological diagnosis of uterine fibroids or uterine sarcomaNot described
Receives: Other: No intervention (observational study)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. AUC

    AUC stands for Area Under the Curve, specifically under the ROC (Receiver Operating Characteristic) curve

    Measured: Histopathological diagnosis obtained from surgical specimens within 1 week after imaging examinations.

  2. Sensitivity

    Ability of the test to correctly identify those with uterine sarcoma (true positive rate)

    Measured: Histopathological diagnosis obtained from surgical specimens within 1 week after imaging examinations.

  3. Specificity

    Ability of the test to correctly identify those without uterine sarcoma (true negative rate)

    Measured: Histopathological diagnosis obtained from surgical specimens within 1 week after imaging examinations.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted8 Dec 2025
  2. Study start30 Sep 2026 (estimated)
  3. Primary completion1 Jan 2050 (estimated)
  4. Study completion1 Jan 2050 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case-control
Time perspective
Prospective
Enrolment
500 participants (estimated)
Target duration
5 Years
IDs, dates and publications
ClinicalTrials.gov ID
NCT07269535
Sponsor's protocol ID
TJ-IRB202511040
Status last verified
Oct 2026
First submitted
26 Nov 2025
Last updated
8 Oct 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Free account

Keep searching with a free account

You’ve used your 3 free searches for this session. Log in or create a free AzTrials account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in