NCT07270237 A Study of Multiparametric Ultrasound Imaging Methods
| NCT ID | NCT07270237 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Memorial Sloan Kettering Cancer Center |
| Condition | Pancreatic Cancer |
| Study Type | INTERVENTIONAL |
| Enrollment | 85 participants |
| Start Date | 2025-11-24 |
| Primary Completion | 2027-11 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 85 participants in total. It began in 2025-11-24 with a primary completion date of 2027-11.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
The researchers are doing this study to see how well a type of ultrasound imaging called multiparametric ultrasound (mpUS), can be used to examine, evaluate, and provide information about different cancerous and non-cancerous tissue. The researchers will compare the results of mpUS imaging to standard ultrasound imaging and other standard tests. mpUS imaging is a type of ultrasound imaging that combines different ultrasound methods and analysis to create a more detailed and accurate assessment of tissue. Standard ultrasound provides a basic image of tissue structure, but mpUS imaging can also show blood vessels, blood flow, and detailed tissue structure (microstructure). The researchers think that mpUS may be a better way for evaluating cancer because it combines different ultrasound methods to assess tissue.
Eligibility Criteria
Inclusion Criteria: * Cohort 1 - Feasibility of multiparametric endoscopic ultrasound (mpEUS) imaging of patients at high-risk for pancreatic cancer: Patient Group: those having standard endoscopic ultrasounds because they are at high risk of pancreatic cancer Participants enrolled into the Memorial Sloan Kettering Cancer Center Pancreatic Registry protocol (IRB#: 02-102) will be eligible for this study. Specifically, related individuals without pancreatic cancer who are at-risk for developing pancreatic cancer and meet all of the following criteria (family health history will be self-reported): * 10 years younger than the earliest pancreatic cancer diagnosis in the family * Be at least 50 years old * Be at least 40 years old if diagnosed with FAMMM syndrome (CDKN2A/p16) or Hereditary Pancreatitis (PRSS1, SPINK1/PST1, CTRC, CPA1 or other candidate hereditary pancreatitis genes) * Be at least 35 years old if diagnosed with Peutz-Jeghers syndrome (STK11 aka LKB1) * Not pregnant and not Nursing * Relatives at least 21 years old with other high-risk clinical criteria that warrants pancreatic cancer surveillance or follow-up as determined by the project leader (Dr. Vineet Rolston) * Must agree to be contacted for follow-up * Must satisfy at least one of the following 4 criteria: 1. Have at least two affected relatives who are a first-degree relative to each other, of whom at least one is a first degree relative to the individual OR have at least two affected first-degree relatives on the same side of the family. 2. Have at least one first- or second-degree affected relative and have germline genetic test results that confirm a likely pathogenic or pathogenic variant in at least one of the following genes: 1. APC (Familial Adenomatous Polyposis (FAP) and Attenuated FAP syndrome 2. BRCA1(Hereditary Breast and Ovarian Cancer Symptoms) 3. MLH1, MSH2, MSH6, PMS2, or EPCAM (Lynch Syndrome) 4. PALB2 5. TP53 (Li-Fraumeni Syndrome) 6. Other established pancreatic cancer predisposition gene per project leader's discretion 3. Have germline genetic test results that confirm a likely pathogenic or pathogenic variant in one or more of the following genes: 1. CDKN2A/p16 (Familial Atypical Multiple Mole Melanoma Syndrome (FAMMM)) 2. STK11 aka LKB1 (Peutz-Jeghers Syndrome) 3. PRSS1, SPINK1/PST1, CTRC, CPA1 or other candidate hereditary pancreatitis genes per project leader's discretion 4. ATM (ataxia telangiectasia mutated) 5. BRCA 2(Hereditary Breast and Ovarian Cancer Symptoms) 4. Relatives at least 21 years old with other high-risk clinical criteria that warrants pancreatic cancer surveillance or follow-up as determined the project leader (Dr. Vineet Rolston) Cohort 2 - Multiparametric endoscopic ultrasound imaging (mpEUS) of patients with pancreatic ductal adenocarcinoma: Patient Group: those with pancreatic cancer having endoscopic ultrasound-guided biopsies Patients will be entered into the study if they meet the following criteria: * Patients with pancreatic ductal adenocarcinoma * Are undergoing endoscopic ultrasound-guided tissue core biopsy as part of their standard of care * Not pregnant and not nursing Cohort 3 - Thyroid nodule assessment with multiparametric ultrasound (mpUS) imaging: Patient Group: those with a thyroid nodule that will be biopsied whether they have known cancer or not * Are undergoing ultrasound-guided thyroid biopsy as part of their standard of care * Not pregnant and not nursing Healthy Volunteers will be entered into the study if they meet the following criteria: * No known cancer diagnosis or thyroid nodules * Age ≥ 18 * Able to understand and give informed consent * Not pregnant and not nursing Exclusion Criteria: Cohort 2 - Multiparametric endoscopic ultrasound imaging (mpEUS) of patients with pancreatic ductal adenocarcinoma: * Unable to sign an informed consent for medical or other reasons; residents outside the continental United States * Under 18 years of age Cohort 3 -Thyroid nodule assessment with multiparametric ultrasound (mpUS) imaging * Unable to sign an informed consent for medical or other reasons; residents outside the continental United States * Under 18 years of age
Contact & Investigator
Mark T Burgess, MD
PRINCIPAL INVESTIGATOR
Memorial Sloan Kettering Cancer Center
Frequently Asked Questions
Who can join the NCT07270237 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, studying Pancreatic Cancer. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07270237 currently recruiting?
Yes, NCT07270237 is actively recruiting participants. Contact the research team at burgesm1@mskcc.org for enrollment information.
Where is the NCT07270237 trial being conducted?
This trial is being conducted at Basking Ridge, United States, Middletown, United States, Montvale, United States, Commack, United States and 3 additional locations.
Who is sponsoring the NCT07270237 clinical trial?
NCT07270237 is sponsored by Memorial Sloan Kettering Cancer Center. The principal investigator is Mark T Burgess, MD at Memorial Sloan Kettering Cancer Center. The trial plans to enroll 85 participants.
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