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The efficacy and safety of different dose and fraction radiation therapy for pancreatic cancer: a prospective, multicenter clinical trial

The efficacy and safety of different dose and fraction radiation therapy for pancreatic cancer: a prospective, multicenter clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800014697
Enrollment
Unknown
Registered
2018-01-30
Start date
2019-02-01
Completion date
Unknown
Last updated
2018-02-05

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

Conditions

pancreatic cancer

Interventions

Conventional dose group:radiotherapy
High-dose group:radiotherapy

Sponsors

The First Hospital of Jilin University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 85 Years

Inclusion criteria

Inclusion criteria: Patients who met all of the following criteria were enrolled: 1. Clinical or pathological confirmed as pancreatic cancer, multi-disciplinary assessment can not surgery or refused surgery; 2. The largest tumor diameter = 7.5cm; 3. ECOG score of 0 -2 points; 4. more than 20 years old, less than 85 years old; 5. To be expected survival of more than 3 months; 6. Blood biochemical tests: bilirubin <1.5 × upper limit of normal (ULN); aspartate aminotransferase or alanine aminotransferase <5 × ULN; serum creatinine <1.0 × ULN; 7. Blood requirements: hemoglobin = 9 g/dL; platelets = 70,000/mL; neutrophils absolute value = 1500/mL; 8. patients with local recurrence of pancreatic cancer after tumor bed; 9. Quasi-radiotherapy site past no history of radiation therapy; 10. Sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. poor health, ECOG score = 3 points; 2. a lot of ascites, or extensive abdominal metastasis; 3. Previous abdomen received external radiotherapy or radioactive I125 particle implantation; 4. are participating in other clinical trials; 5. Gestational or lactating women; 6. There are serious neurological diseases, can not clearly tell the treatment responders.

Design outcomes

Primary

MeasureTime frame
overall survival;progression-free survival;

Secondary

MeasureTime frame
Objective Response Rate;Toxic and side effects;

Countries

China

Contacts

Public ContactDong Lihua

The First Hospital of Jilin University

drlhdong@163.com+86 15843073216

Outcome results

None listed

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