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Construction of Training Datasets for an AI-Assisted Precision Diagnosis and Treatment System for Cholangiocarcinoma and a Prospective, Multicenter, Randomized Controlled Clinical Trial Based on This System

Construction of Training Datasets for an AI-Assisted Precision Diagnosis and Treatment System for Cholangiocarcinoma and a Prospective, Multicenter, Randomized Controlled Clinical Trial Based on This System

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600125974
Enrollment
Unknown
Registered
2026-06-01
Start date
2026-06-01
Completion date
Unknown
Last updated
2026-06-08

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

Conditions

Cholangiocarcinoma

Interventions

Non-AI Assisted Diagnosis and Treatment Group:Non-AI Assisted Diagnosis or Treatment
AI Assisted Diagnosis and Treatment Group:AI Assisted Diagnosis and Treatment
Observation group:None

Sponsors

The second affiliated hospital of Zhejiang University school of medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Patients aged 18 to 80 years old; 2.Preoperative imaging and laboratory examinations suggest cholangiocarcinoma, confirmed by postoperative pathology (surgical patients) or puncture pathology (non-surgical patients); 3.Patients have autonomous capacity, understand and voluntarily sign written informed consent, and can complete the follow-up plan; 4.Signed written informed consent before trial screening;

Exclusion criteria

Exclusion criteria: 1.Patients with obvious cardiac, pulmonary, cerebral or renal insufficiency that affects the management of cholangiocarcinoma; 2.Patients with a history of other malignant tumors; 3.Patients deemed unsuitable for this study by the investigator;

Design outcomes

Primary

MeasureTime frame
R0 resection rate in surgical patients;Tumor progression-free rate and disease response rate in non-surgical patients;Diagnostic accuracy of preoperative lymph node metastasis;

Secondary

MeasureTime frame
3-year disease-free survival rate;30-day major complication rate after surgery;Surgical operation and postoperative recovery indicators;3-year overall survival rate;Tumor marker decline rate in non-surgical patients;

Countries

China

Contacts

Public ContactJiangtao Li

The second affiliated hospital of Zhejiang University school of medicine

zjuljt@gmail.com+86 136 6665 1245

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026