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the safety and effect of endoscopic combined with immunotherapy on unresectable hilar cholangiocarcinoma

the safety and effect of endoscopic combined with immunotherapy on unresectable hilar cholangiocarcinoma

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000039682
Enrollment
Unknown
Registered
2020-11-05
Start date
2020-11-09
Completion date
Unknown
Last updated
2021-02-16

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

Conditions

hilar cholangiocarcinoma

Interventions

experimental group:Radiofrequency ablation + biliary stent implantation + immunotherapy
control group:Radiofrequency ablation + biliary stent implantation

Sponsors

The First Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Aged >= 18 years; 2. CT and MRI diagnosis should be confirmed by pathology or histology as far as possible; 3. Clinical jaundice, bilirubin > 5mg/dL, with or without cholangitis; 4. Patients with local macrovascular infiltration or distant metastasis indicated by color ultrasound, CT or MRI, and who could not be surgically removed or refused to be surgically removed after discussion by the expert group; 5. Those who have been diagnosed for the first time; 6. Patients willing to undergo endoscopic combined immunotherapy and long-term follow-up.

Exclusion criteria

Exclusion criteria: 1. Severe biliary tract infection; 2. Severe cardiopulmonary diseases, unable to tolerate surgery; 3. Patients with other malignant tumors; 4. Severe liver dysfunction (prothrombin time 442umol/L); 5. Other treatments that may affect the follow-up results: seed stent implantation, chemoradiotherapy, etc.Refusal of endoscopic therapy or withdrawal during immunotherapy; 6. Benign and malignant tumors of the pancreas, biliary tract and duodenum; 7. Failure in surgery; 8. Participate in other researchers.

Design outcomes

Primary

MeasureTime frame
median overall survival;

Secondary

MeasureTime frame
KPS score changes;Stent patency time;progression free survival time;adverse effects;death reasons;

Countries

China

Contacts

Public ContactWu Qiao

The First Affiliated Hospital of Chongqing Medical University

wuqiao001268@163.com+86 13983765868

Outcome results

None listed

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