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Establishment of Radiomics Database by Clinical Application of Multiparametric MRI Based on Incoherent Undersampling

Establishment of Radiomics Database by Clinical Application of Multiparametric MRI Including DCE-MRI Based on Incoherent Undersampling

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02944006
Enrollment
29
Registered
2016-10-25
Start date
2016-11-28
Completion date
2023-11-30
Last updated
2021-12-17

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

Conditions

Pancreas Cancer

Keywords

MRI

Brief summary

This study aims to establish radiomics database for pancreas cancer from multiparametric MRI including DCE-MRI obtained by using incoherent undersampling and radial acquisition for clinical staging as well as quantitative analysis.

Interventions

multiparametric MRI is performed in all patients, and the sequence includes dynamic contrast enhanced (DCE) MRI, diffusion weighted imaging (DWI), tissue maps, and MR cholangiography.

Sponsors

Seoul National University Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* surgical candidate for pancreatico-duodenectomy * characteristic finding of pancreatic adenocarcinoma on prior CT or MRI * OR histologically diagnosed with pancreatic adenocarcinoma * signed for informed consent

Exclusion criteria

* under 18 years * not eligible for pancreatico-duodenectomy * unresectable patients (locally advanced on prior CT/MRI or metastatic disease) * tumors with suspicion of other histologic types (neuroendocrine, IPMN, etc) * any contra-indication of contrast-enhanced MRI * recurred pancreatic cancer

Design outcomes

Primary

MeasureTime frameDescription
T-staging4 weeks after MR acquisitionT-staging of the tumor at MRI.

Secondary

MeasureTime frameDescription
arterial blood flow4 weeks after MR acquisitionarterial blood flow of the tumor and adjacent parenchma on DCE-MRI
arterial fraction4 weeks after MR acquisitionarterial fraction of the tumor and adjacent parenchyma on DCE-MRI
mean transit time4 weeks after MR acquisitionmean transit time of the tumor and adjacent parenchyma on DCE-MRI
extracellular volume4 weeks after MR acquisitionextracellular volume of the tumor and adjacent parenchyma on DCE-MRI
true diffusion4 weeks after MR acquisitiontrue diffusion of the tumor and adjacent parenchyma on DWI with intravoxel incoherent motion model
pseudodiffusion4 weeks after MR acquisitionpseudodiffusion of the tumor and adjacent parenchyma on DWI with intravoxel incoherent motion model
perfusion fraction4 weeks after MR acquisitionperfusion fraction of the tumor and adjacent parenchyma on DWI with intravoxel incoherent motion model
kurtosis4 weeks after MR acquisitionkurtosis of the tumor and adjacent parenchyma on DWI with kurtosis model
mean diffusivity4 weeks after MR acquisitionmean diffusivity of the tumor and adjacent parenchyma on DWI with kurtosis model
N-staging4 weeks after MR acquisitionN-staging of the tumor at MRI

Other

MeasureTime frameDescription
T1 value4 weeks after MR acquisitionT1 value of the tumor and adjacent parenchyma using T1 map
T2 value4 weeks after MR acquisitionT1 value of the tumor and adjacent parenchyma using T2 map
fat fraction4 weeks after MR acquisitionfat fraction of the tumor and adjacent parenchyma using T2\* corrected fat map
global textural feature4 weeks after MR acquisitionfirst order parameters related to the grey level frequency distribution in the region of interest using dedicated software
local textural feature4 weeks after MR acquisitionsecond order parameters calculated with spatial grey level dependence matrices or co-occurrence matrices using dedicated software
attenuation4 weeks after MR acquisitionhounsefield unit (HU) of the tumor and parameter on CT within 4 weeks of MRI
transient dyspnea1 day after MR acquisitiondevelopment of transient dyspnea or involuntary motion after contrast media administration

Countries

South Korea

Outcome results

None listed

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