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A CSD precision diagnosis and treatment prediction model based on clinical-imaging multimodal data

A CSD precision diagnosis and treatment prediction model based on clinical-imaging multimodal data

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600122974
Enrollment
Unknown
Registered
2026-04-20
Start date
2026-04-20
Completion date
Unknown
Last updated
2026-04-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Uterine scar defect

Interventions

Observation group:None

Sponsors

Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. History of cesarean section, and more than 3 months post-surgery; with or without clinical symptoms; ultrasound and MRI examinations indicate myometrial defect or uterine wall niche at the cesarean scar site, clinically diagnosed as patients with cesarean scar defect; 2. Patients who were diagnosed with cesarean scar defect by imaging at this center and, after assessment by senior physicians, decided to undergo conservative treatment or transvaginal repair surgery; 3. Complete pre-treatment clinical text data and original imaging data; 4. For surgical patients: must have ultrasound follow-up data at 3 months and 6 months post-surgery, and MRI follow-up data at 6 months post-surgery; 5. No serious internal medical conditions (vital organ functions within normal range); 6. No history of malignant tumors.

Exclusion criteria

Exclusion criteria: 1.The diagnostic criteria were not fully met, and the imaging basis was not satisfied. 2.The clinical text data or imaging images are incomplete, making it impossible to extract the required variables. 3.Having severe internal medical conditions (severe liver disease, kidney disease, respiratory diseases, heart diseases or diabetes, epilepsy, etc., with abnormal functions of important organs); 4.Patients with malignant tumors combined. 5.Patients with regnancy state; 6.The quality of the imaging images is not satisfactory, including severe blurring and incomplete sequences, etc.

Design outcomes

Primary

MeasureTime frame
optimal/suboptimal outcomes;

Secondary

MeasureTime frame
pregnancy outcome;

Countries

China

Contacts

Public ContactXipeng Wang

Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine

wangxipeng@xinhuamed.com+86 21 2507 8999

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 1, 2026