Actively Recruiting

Phase 3
Age: 18Years - 99Years
All Genders
NCT06391892

Liquid Biopsy (ctDNA) Guided Treatment in Localized Pancreatic Cancer: Neoadjuvant CTX vs. Upfront Surgery

Led by Elisabethinen Hospital · Updated on 2024-04-30

100

Participants Needed

1

Research Sites

155 weeks

Total Duration

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Sponsors

E

Elisabethinen Hospital

Lead Sponsor

M

Medical University Innsbruck

Collaborating Sponsor

AI-Summary

What this Trial Is About

This study evaluates the clinical prognostic impact (on DFS and OS) of liquid biopsy guided treatment vs. standard of care (physicians choice) in localized pancreatic cancer (despite because of CA 19-9 levels and computed tomography, upfront surgery is recommended by tumor board). ctDNA positive patients will receive neoadjvuant chemotherapy at current gold standard physicians choice instead of upfront surgery, because of assumed high biological risk for early recurrence.

CONDITIONS

Official Title

Liquid Biopsy (ctDNA) Guided Treatment in Localized Pancreatic Cancer: Neoadjuvant CTX vs. Upfront Surgery

Who Can Participate

Age: 18Years - 99Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Informed consent
  • Age greater than 18 years
  • Diagnosed with localized pancreatic cancer recommended for upfront surgery
Not Eligible

You will not qualify if you...

  • Having a synchronous secondary malignancy
  • Being pregnant

AI-Screening

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Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Ordensklinikum Linz Barmherzige Schwestern

Linz, Upper Austria, Austria, 4010

Actively Recruiting

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Research Team

P

Patrick Kirchweger, MD, PhD

CONTACT

H

Helwig Wundsam, PD, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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