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Clinical research for the application of DWI, ctDNA to predict the outcomes after liver tumor alblation

Clinical research for the application of DWI, ctDNA to predict the outcomes after liver tumor alblation

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900028075
Enrollment
Unknown
Registered
2019-12-10
Start date
2018-10-18
Completion date
Unknown
Last updated
2019-12-16

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

Conditions

colorectal cancer with liver metastasis

Interventions

Sponsors

Fudan University Shanghai Cancer Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Have a liver metastatic colorectal cancer diagnosed by cytology, histology, or radiology; 2. Have an Karnofsky performance status (PS) >=70; 3. Metastatic liver tumors are able to be radically ablated: single tumor with maximum diameter =1500/uL; Hemoglobin>=8 g/dL; Platelets>=80,000/uL; Creatinine=18 years of age, at the time of signing the informed consent; 8. The participant (or legally acceptable representative if applicable) provides written informed consent/assent for the study.

Exclusion criteria

Exclusion criteria: 1. Have contraindications for liver tumor ablation or unable to do radical ablation; 2. Need to combine with other local treatment for metastatic liver tumors, such as radiation; 3. Have central neural system disease and pia mater disease; 4. Have other serious disease, such as congestive heart-failure (Grade III or IV according to the New York heart association grading system); unstable angina; myocardial infarction within the last 6 months; serious arrhythmia; QT prolongation; HIV infection; mental disorders; drug abuse; 5. Have infection which needs intravenous antibiotic treatment; 6. A female participant who is pregnant or breastfeeding. Participants Reject contraception during the study; 7. Have second primary malignancy; 8. Allergic to CT or MRI contrast agents; 9. Participants of poor compliance.

Design outcomes

Primary

MeasureTime frame
ctDNA;

Secondary

MeasureTime frame
tumor mutation burden;

Countries

China

Contacts

Public ContactMeng Zhiqiang

Fudan University Shanghai Cancer Center

mengzhq@yeah.net+86 13901711875

Outcome results

None listed

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