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NCT06126159Active, not recruiting

MRI Functional Imaging Characteristics and Fat Quantification of CT-fat-free Renal Neoplasms: Relationships With Histological Classifications and Molecular Markers

Source: ClinicalTrials.gov · Last updated 20 Mar 2026

Brief summary (registry, in English)

The knowledge of the histological diagnosis and its subtype of a renal parenchymal tumor is important for determine whether the choice of a specific regimen of chemotherapy, target therapy and immunotherapy could be suitable and effective for treating this tumor. Computed tomography (CT) has been considered as an excellent imaging modality for detecting intra-tumoral fat, and most of renal angiomyolipomas (AML) could be thus confidently diagnosed on computed tomography by showing intra-tumoral fat. However, if a renal parenchymal tumor has no detectable fat in the tumor on computed tomography, there is a long list of its diagnosis including benign neoplasms as angiomyolipoma with minimal fat, oncocytoma, metanephric adenoma, etc., epitheloid angiomyolipoma (eAML) malignant potential, malignant neoplasms as renal cell carcinoma (RCC), sarcoma, malignant eAML, etc. Furthermore, there are three kinds of anticancer drug (antiangiogenetic drug, mammalian target of rapamycin inhibitors, immune modulators, and whether the anticancer drug is effective mainly depending on subtypes of RCCs. Nonetheless, computed tomography could not reliably differentiate histological types of renal parenchymal masses except renal AMLs with abundant fat. Therefore, for patients without established diagnoses by imaging examinations, further biopsy of the renal tumor is usually mandatory to validate the histological diagnosis and subtype. Thus, this study plans to enroll 60 patients with renal parenchymal masses which show no intra-tumoral fat on computed tomography. All enrolled patients will undergo multiparametric and fat-detection magnetic resonance imaging (MRI).

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
44 (estimated)
First submitted
6 Nov 2023
Start date
11 Feb 2019
Primary completion date
31 Dec 2026
Lead sponsor
Chang Gung Memorial Hospital
NCT number
NCT06126159

What you commit to

  • Study type: Interventional
  • Planned participants: 44
  • From 11 Feb 2019 to the primary completion date, 31 Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Pregnant or lactating woman
  • Withdrawal of informed consent
  • Those who have not completed MRI
  • Those who did not receive renal tumor biopsy

Who the study is looking for

  • Age ≥ 20 years old
  • Have renal parenchymal masses with no detectable intra-tumoral fat on computed tomography (CT)
  • Normal renal function (i.e.: estimated glomerular filtration rate ≧ 60 mL/min/1.73 m2)
  • No allergy history of iodinated contrast medium

Age in the registry: 20 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Li-Jen Wang
Coordinator of this site? Confirm its status
TaoyuanTaiwanUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.