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Iodine-125 seed brachytherapy combined with chemotherapy for locally advanced pancreatic cancer- A multicenter prospective cohort study

Iodine-125 seed brachytherapy combined with chemotherapy for locally advanced pancreatic cancer- A multicenter prospective cohort study

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000032070
Enrollment
Unknown
Registered
2020-04-19
Start date
2020-05-01
Completion date
Unknown
Last updated
2020-04-20

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

Conditions

Pancreatic cancer

Interventions

Experimental group:Iodine-125 seed implantation plus chemotherapy
Control group:Chemotherapy

Sponsors

The Second Hospital of Shandong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Age: 18-80 years old, gender unlimited; 2. Patients with pancreatic cancer confirmed by histopathology; 3. Patients with locally advanced pancreatic cancer confirmed by imaging (enhanced CT / enhanced MR); 4. Patients without systemic metastasis; 5. Patients with expected survival time >=3 months; 6. Patients with ECoG score <=2; 7. Patients who did not receive radiotherapy, chemotherapy or molecular targeted therapy within one month before treatment; 8. Patients willing to participate in this study and sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with distant metastasis or other malignancies besides pancreatic cancer; 2. Patients with WBC count <=3.0x10^9/L; 3. Patients with platelet count <=50x10^9/L; 4. Patients with coagulation dysfunction; 5. Patients with serious diseases of heart, lung, brain, liver, kidney and other important organs; 6. Patients with mental disorder or mental history; 7. Patients with abnormal thyroid function; 8. Patients with acute or chronic infection; 9. The investigator confirmed that the patients are not suitable for the group.

Design outcomes

Primary

MeasureTime frame
Overall Survival;

Secondary

MeasureTime frame
PFS;ORR;DCR;

Countries

China

Contacts

Public ContactYuliang Li

The Second Hospital of Shandong University

lyl.pro@sdu.edu.cn+86 15153169899

Outcome results

None listed

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