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A Study of Multiparametric Ultrasound Imaging Methods

Development and Evaluation of Ultrasound Imaging Acquisition and Analysis Methods

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07270237
Enrollment
85
Registered
2025-12-08
Start date
2025-11-24
Completion date
2027-11-30
Last updated
2025-12-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pancreatic Cancer, Thyroid Nodule

Keywords

Ultrasound, mpUS, 25-299

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.

Interventions

DIAGNOSTIC_TESTMultiparametric ultrasound (mpUS) imaging

Patients will undergo the added research sequences at any point during their standard of care ultrasound scans, adding up to approximately 15 minutes of added scan time. The only non-routine measurements will be the research ultrasound data.

Sponsors

Memorial Sloan Kettering Cancer Center
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
investigate the feasibility of mpEUS imaging1 daythe feasibility rate will be estimated and reported using the corresponding sample proportion, along with exact binomial 95% confidence intervals. The mpEUS technique will be considered feasible if it is able to visualize/quantify parameters in at least 21 patients out of the 30 patients.

Countries

United States

Contacts

Primary ContactMark T Burgess, PhD
burgesm1@mskcc.org646-608-8284
Backup ContactWyanne Law, MD
laww@mskcc.org

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026