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A prospective, multicenter, controlled study protocol of the interactive assisted delineation software for CT radiotherapy in breast cancer CTV

A prospective, multicenter, controlled study protocol of the interactive assisted delineation software for CT radiotherapy in breast cancer CTV

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400091358
Enrollment
Unknown
Registered
2024-10-28
Start date
2024-10-28
Completion date
Unknown
Last updated
2024-11-04

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

Conditions

breast cancer

Interventions

Control group (hand-drawn):NA
Experimental Group (Interactive AI-assisted sketching):NA

Sponsors

Southern Medical University Southern Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients aged 18 and above; 2. Patients diagnosed with breast cancer need to receive postoperative adjuvant radiotherapy, which may include adjuvant radiotherapy of the breast gland, chest wall, clavicle, and internal mammary lymph nodes. 3. Supine positioning CT, image slice thickness = 5 mm; 4. Consider the patient age and surgical procedure from the perspective of distribution to ensure that the age and surgical procedure distribution of the included subjects is close to the clinical reality.

Exclusion criteria

Exclusion criteria: 1. Congenital malformation or anatomical abnormality of the scanned area; 2. The patient's position does not meet common clinical scanning standards; 3. Artifacts, prostheses, implants, etc. make the image unclear and difficult to distinguish; 4. Images do not conform to the DICOM standard; 5. The researcher considers it inappropriate;

Design outcomes

Primary

MeasureTime frame
Dice Similarity Coefficient;sketch time;

Countries

China

Contacts

Public ContactLongmei Cai

Southern Medical University Southern Hospital

cailongmeibestlove@163.com+86 13450205073

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026