Using contrast-enhanced ultrasound to check for local pancreatic cancer recurrence after surgery
Official title: The Use of Contrast Enhanced Ultrasound (CEUS) In Post-Surgical Pancreatic Cancer Patients to Evaluate Local Disease Recurrence- A Feasibility Study
Run by Thomas Jefferson University · NCT07910383 · Data updated 2026-11-12
This pilot test uses contrast-enhanced ultrasound to see if it can help detect return of pancreatic cancer after surgery in patients being watched with CT scans.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 10 (estimated) |
| Sponsor | Thomas Jefferson University Academic / other |
| Locations | 1 site (Philadelphia, Pennsylvania) |
| Status | Recruiting |
| Started | July 29, 2026 |
| Main results expected | December 2026 |
| Study ends | December 2026 |
| Registry record updated | November 2, 2026 |
| Trial ID | NCT07910383 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adults who had surgical resection of PDAC in the head or body of the pancreas and are undergoing ongoing CT-based surveillance for recurrence.
✕Probably not a fit
Patients with non-local (distant) recurrence or those not having a recurrence on standard imaging may not receive additional diagnostic benefit from CEUS.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This is a small, nonrandomized pilot study enrolling up to 10 adults who previously had surgical resection of pancreatic ductal adenocarcinoma and are being monitored for recurrence. Investigators will use a Logiq E10 ultrasound with contrast to image the area of the original surgery to see if CEUS can identify local recurrence. The study will compare CEUS findings against standard imaging results to assess practicality and potential utility. CEUS contrast agents are expected to enhance imaging signals with favorable safety, though the most serious risk is rare anaphylactic reaction. No treatment is administered; the goal is to determine whether CEUS can help detect local disease.
Why it matters
Potential benefit: If successful, CEUS could provide a simpler, safer way to detect local recurrence after PDAC surgery.
How similar studies have gone: Previous experiences with CEUS show promise in detecting focal lesions and may be translational to pancreatic imaging in specialized centers, but direct validation for post-surgical pancreatic recurrence is limited.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria:
* Individuals must meet all of the following inclusion criteria in order to be eligible to participate in the study:
1. Be a patient that underwent surgical resection of PDAC located in the head or body of the pancreas and are being followed for recurrence with CT imaging as part of their standard of care.
2. Be 18 years of age or older.
3. If the subject is of child-bearing potential, must have a negative pregnancy test.
4. Be conscious and able to comply with study procedures.
5. Have read and signed the IRB approved consent form for participating in the study.
Exclusion Criteria:
* An individual who meets any of the following criteria will be excluded from participation in this study:
1. Females who are pregnant or nursing.
2. Patients who have received an investigational drug in the 30 days before study drug administration or will receive one within 72 hours afterwards.
3. Patients who are medically unstable, patients who are seriously or terminally ill, and patients whose clinical course is unpredictable. For example:
* Patients on life support or in a critical care unit.
* Patients with clinically unstable cardiopulmonary conditions (acute myocardial infarction, acute coronary artery syndromes, worsening or unstable congestive heart failure, or serious ventricular arrhythmias)
* Patients with recent cerebral hemorrhage (within 1 month).
4. Patients who have undergone surgery within 24 hours prior to the study ultrasound imaging examination.
5. Patients with congenital heart defects.
6. Patient with a known allergy to Lumason.
Where it's running
-
Sidney Kimmel Comprehensive Cancer Center at Thomas Jefferson University
Philadelphia, Pennsylvania, United States Recruiting
Study contacts
- Principal investigator: Priscilla Machado, MD, FAIUM — Sidney Kimmel Comprehensive Cancer Center at Thomas Jefferson University
- Study coordinator: Site Public Contact
- Email: ONCTrialNow@jefferson.edu
- Phone: 215-600-9151
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.