Actively Recruiting
ctDNA Assay in Patients With Resectable Pancreatic Cancer
Led by University of Oklahoma · Updated on 2026-03-05
50
Participants Needed
2
Research Sites
340 weeks
Total Duration
On this page
Sponsors
U
University of Oklahoma
Lead Sponsor
N
Natera, Inc.
Collaborating Sponsor
AI-Summary
What this Trial Is About
The purpose of this study is to determine the proportion of positive ctDNA -freely circulating tumor DNA fragments found in the blood plasma- in patients with pancreatic cancer and to better understand the relationship between possible ctDNA biomarkers and patient survival. A successful study may provide preliminary evidence that helps improve future patient care through targeted diagnostics, prognosis, and/or treatment.
CONDITIONS
Official Title
ctDNA Assay in Patients With Resectable Pancreatic Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Newly diagnosed exocrine pancreatic cancer confirmed by pathology or imaging
- Resectable or borderline resectable pancreatic cancer as defined by NCCN guidelines
- At least 18 years old at the time of informed consent
- ECOG Performance Status of 0 or 1
- Eligible for neoadjuvant chemotherapy, chemoradiotherapy, or upfront surgery
- Able to provide written informed consent and HIPAA authorization
- Life expectancy of at least 6 months
You will not qualify if you...
- Pancreatic tumors confirmed as neuroendocrine or other types of malignancies
- Positive pregnancy test, pregnant, or breastfeeding
- Any significant and/or uncontrolled cardiac abnormality compromising safety or study outcome
- Locally advanced or metastatic pancreatic cancer
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 2 locations
1
University of Oklahoma
Oklahoma City, Oklahoma, United States, 73117
Actively Recruiting
2
Stephenson Cancer Center- Tulsa
Tulsa, Oklahoma, United States, 74104
Not Yet Recruiting
Research Team
L
Lead Nurse
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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