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Development of an AI Model Based on Retrospective Pelvic Imaging for Adenomyosis Subtype Identification

Construction of a Female Pelvic Foundation Model Driven by Retrospective Pelvic Imaging Data and Automated Classification of Adenomyosis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600131521
Enrollment
Unknown
Registered
2026-09-03
Start date
2026-09-03
Completion date
Unknown
Last updated
2026-09-07

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

Conditions

Adenomyosis

Interventions

Gold Standard:Multi-reader Imaging Expert Consensus

Sponsors

Obstetris & Gynecology Hospital of Fudan University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
14 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Female patients aged > 14 years and non-obstetric/non-puerperal; 2.Underwent pelvic MRI or CT examination at a participating institution; 3.Imaging data were complete, with image quality sufficient for diagnostic interpretation and model training; 4.Complete clinical medical records were available( including diagnosis, surgical or pathological records, imaging follow-up, etc.).

Exclusion criteria

Exclusion criteria: 1.Image quality was severely compromised, precluding use for model training or validation; 2.Incomplete data with critical clinical information missing; 3.Incomplete de-identification with potential patient re-identification risk (to be verified by the institutional information technology department); 4.The patient had explicitly submitted a data use refusal declaration to the hospital within the valid period (if applicable); 5.Patients with a history of prior total hysterectomy (unless serving as a source of pathological gold standard for reference standard establishment); 6.Patients with other pelvic pathologies that significantly affect the interpretation of uterine morphology (e.g., giant uterine fibroids, uterine malformations), to be analyzed separately as a subgroup and excluded from the primary analysis set.

Design outcomes

Primary

MeasureTime frame
Diagnostic performance analysis;Consistency and reliability analysis;

Countries

China

Contacts

Public ContactXiaofang Yi

Obstetris & Gynecology Hospital of Fudan University

yixiaofang1433@fckyy.org.cn+86 21 33189900

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Sep 19, 2026