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Clinical Study for Small Diameter Drug-Eluting Beads(70-150µm) TACE Treatment for Unresectable mass forming intrahepatic cholangiocarcinoma

Clinical Study for Small Diameter Drug-Eluting Beads(70-150µm) TACE Treatment for Unresectable mass forming intrahepatic cholangiocarcinoma

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400086108
Enrollment
Unknown
Registered
2024-06-25
Start date
2024-06-30
Completion date
Unknown
Last updated
2024-07-08

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

Conditions

Unresectable mass-forming intrahepatic cholangiocarcinoma

Interventions

Observation group (TACE treatment with small diameter Drug-Eluting Beads(70-150µm) ):None

Sponsors

Beijing Tsinghua Changgung Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1)mass-forming intrahepatic cholangiocarcinoma was clinical diagnosed; 2)Patients who were evaluated by 2 associate senior hepatobiliary surgeons or above for patients who could not be surgically resected or who failed first-line systemic chemotherap; 3)ECOG PS 0-1; 4)Good liver function(Child grade A\B); 5)Life expectancy = 3 months; 6)Aged 18-75 years; 7)Signed informed consent;

Exclusion criteria

Exclusion criteria: 1) Severe active infection greater than grade 2 (except hepatitis B or C infection); 2) With malignant tumors of other organs; 3) Severe heart, lung and kidney diseases; 4) Pregnant or lactating women; 5) Those who have severe neurological lesions and can not clearly describe the response of treatment; 6) Patients with severe atherosclerosis; 7) AIDS patients; 8) Patients with severe gastrointestinal bleeding within 4 weeks; 9) Severe thrombosis or emboli within 6 months; 10) Is participating in other clinical trials or is preparing to participate in other clinical trials; 11) Patients who are considered inappropriate by the investigator (poor compliance and cannot be followed-up)

Design outcomes

Primary

MeasureTime frame
Progression-free survival;

Secondary

MeasureTime frame
Median Survival Time;Time To Progress;Survival Rate of 6.12.18 month;Tumor responses;

Countries

China

Contacts

Public ContactLiu Ying

Beijing Tsinghua Changgung Hospital

lya02340@btch.edu.cn+86 173 2685 3673

Outcome results

None listed

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