Actively Recruiting
Radiotherapy for Locally Advanced Pancreatic Carcinomas (Phase II Trial)
Led by EBG MedAustron GmbH · Updated on 2026-03-20
30
Participants Needed
1
Research Sites
341 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This is an interventional, single-arm, open-label study with high dose short course radiotherapy for patients with locally advanced pancreatic cancer.
CONDITIONS
Official Title
Radiotherapy for Locally Advanced Pancreatic Carcinomas (Phase II Trial)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Histologically or cytologically confirmed pancreatic cancer, or radiological suspicion with elevated CA 19-9
- Patient is not a candidate for radical surgical resection due to locally advanced unresectable disease or progression during neoadjuvant chemotherapy or cN+ stage
- Patient is not a candidate for further neoadjuvant chemotherapy due to unfitness, progression, or unsuitability for surgery
- No distant metastasis detected
- Age over 18 years
- Karnofsky performance status of 70 or higher
- No tumor invasion into stomach or duodenum
- Patient understands the diagnosis and can give informed consent
- Women of childbearing potential use effective contraception and do not breastfeed
- Signed informed consent available before inclusion
You will not qualify if you...
- Non-exocrine pancreatic tumors
- Major medical or psychiatric conditions preventing radiotherapy
- Presence of distant metastasis
- Pregnancy or unwillingness to use contraception
- Lactating and unwilling to stop breastfeeding
- Men unwilling to use effective contraception
- Metallic prosthesis or other conditions preventing adequate imaging for treatment planning
- Previous abdominal radiotherapy
- Severe liver or kidney impairment
- Patient refusal to participate
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
EBG MedAustron GmbH
Wiener Neustadt, Lower Austria, Austria, 2700
Actively Recruiting
Research Team
P
Piero Fossati, M.D.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
OTHER
Number of Arms
1
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