DCE-MRI Guided Neoadjuvant Chemotherapy for Borderline Resectable Pancreatic Cancer

Part of paid clinical trials in Indianapolis, Indiana.

Sponsor
Ohio State University
Study ID
NCT06173310
Status
Recruiting

Conditions

  • Borderline-resectable Pancreatic Cancer

Eligibility Criteria

Sex
ALL
Age
19 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Point-of-care Portable Perfusion Phantom (P4) — DEVICE
    P4 is a perfusion phantom developed by Dr. Harrison Kim that can significantly reduce variation in quantitating perfusion of human abdominal tissues across MRI scanners.

Study Details

The goal of this study is to test whether chemotherapy guided by a new imaging method named DCE-MRI can more effectively reduce a pancreatic tumor, enabling curable surgery, over the conventional method when a tumor is categorized as borderline resectable pancreatic cancer. UAB radiological research team has been studying a cutting-edge imaging technique named dynamic contrast-enhanced magnetic resonance imaging, or DCE-MRI, for over 10 years. This technique has been globally used to calculate the blood flow of various tissues, including tumors. Blood flow often serves as a critical indicator showing a disease status. For example, a pancreatic tumor typically has low blood flow, so it can be used as an indicator to identify the presence of a pancreatic tumor. In addition, an effective therapy can result in the increase of blood flow in a pancreatic tumor during the early period of treatment. Therefore, the investigators may be able to determine whether the undergoing therapy is effective or not by measuring the change of blood flow in the pancreatic tumor and deciding whether to continue the therapy or try a different one.

Key Dates

Start date
Oct 10, 2024
Status verified
Feb 2025
Primary completion
Mar 31, 2029
Completion
Mar 31, 2029

Study Design

Enrollment
50 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC

Arms

  • Experimental: borderline-resectable pancreatic cancer (BRPC)

Primary Outcome Measure

To measure the reproducibility of qDCE-MRI measurement of BRPC. [ Time Frame: 6 weeks +/- 2 weeks ]

Central Contacts

Locations (2)

FacilityCityStateZIPSite coordinators
Indiana University Medical CenterIndianapolisIndiana46202
D D
5555555555
Asiq Masood, MD (PRINCIPAL_INVESTIGATOR)
Jordan Swensson, MD (SUB_INVESTIGATOR)
Yu-Chien Wu, MD (SUB_INVESTIGATOR)
Omer Saeed, MD (SUB_INVESTIGATOR)
The Ohio State UniversityColumbusOhio43210
Tamara Stein, MPH
614-293-8315
Harrison Kim, PhD (PRINCIPAL_INVESTIGATOR)

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