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RecruitingNCT04623502Updated Jan 28, 2026

An Investigation of Kidney and Urothelial Tumor Metabolism in Patients Undergoing Surgical Resection and/or Biopsy

An interventional study of 13C-Glucose and 13C-Acetate in Kidney Cancer, Renal Cell Carcinoma and Clear Cell Carcinoma, sponsored by University of Texas Southwestern Medical Center. Recruiting at 1 site in United States. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-01-28.

Sponsored by University of Texas Southwestern Medical Center · Not applicable, Interventional, and Basic science

Phase
Not applicable
Study type
Interventional
Enrollment
600
Allocation
Non-randomized
Ages
18 Years and older
Sex
All
01

Study summary

The purpose of this study is to understand the metabolism of cancers involving the kidney, including renal cell carcinomas and urothelial cell carcinomas, and how kidney cancers use different types of fuel to support tumor growth. This study uses specially labeled nutrient tracers of compounds normally found circulating in the blood. The nutrients (glucose, fructose, glutamine, acetate, and lactate) are also found in common foods. A nutrient tracer will be given to the participants through an intravenous (IV) catheter during surgery or biopsy, and blood will be collected every 30 minutes during the infusion to monitor safety parameters and the nutrient tracers. The investigators will collect a tissue sample after the completion of surgery. Participants not having an infusion will have their tissue collected after surgery or biopsy.

Participation in this study will not change patient care. All patients will receive standard of care treatment as determined by their doctors.

Read the detailed description

The purpose of this study is to understand the metabolism of kidney cancers (renal cell carcinomas and urothelial cell carcinomas involving the kidney) in patients. Metabolism is the term used to describe how cells take up different nutrients and convert them to energy and materials needed for cell growth. In cancer, metabolism is hijacked to support the needs of cancer cells. Cancer cells can use multiple nutrients in the blood to fuel their growth, but it is not known what materials cancer cells make with those nutrients in patients.

Many participants in this study will be infused with a 13C-labeled nutrient during their surgery or biopsy. 13C means that the carbon in the nutrient is heavier than 12C carbons that are the most abundant carbon atoms in nature. 13C carbons account for about 1% of natural carbon atoms are not radioactive or harmful in any way. Using the tissue collected during or after surgery and/or biopsy, the researchers can track how the heavier 13C carbons from the infused nutrient are being used to make different materials that cancer cells need to grow.

The researchers hope to understand how kidney cancers change their metabolism to adapt, grow, and survive in patients. The knowledge learned from this study will be used to support the development of therapies that target metabolic adaptations, and the development of new non-invasive imaging techniques that will improve the care and survival of future kidney cancer patients.

02

Conditions studied

  • Kidney Cancer
  • Renal Cell Carcinoma
  • Clear Cell Carcinoma
  • Urothelial Carcinoma
  • Metastatic Kidney Cancer
  • Metastatic Urothelial Carcinoma
  • Papillary Renal Cell Carcinoma
  • Chromophobe Renal Cell Carcinoma
  • Fumarate Hydratase Deficiency
  • Succinate Dehydrogenase-Deficient Renal Cell Carcinoma
  • HLRCC
  • Hereditary Leiomyomatosis and Renal Cell Cancer
03

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Patients must have radiographic evidence of known or probable kidney or urothelial cancer requiring surgical biopsy or excision.
  • Age ≥ 18 years
  • Subjects of all races and ethnic origins
  • The willingness to sign and ability to understand a written informed consent.
  • Patients participating in other clinical trials are eligible, and will be evaluated on a case by case basis by the Principal Investigator, Dr. Vitaly Margulis, MD.

Exclusion criteria

Exclusion Criteria:

  • Uncontrolled or poorly controlled diabetes for patients receiving a 13C infusion
  • Pregnant or breastfeeding
  • Not a surgical candidate
04

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
600 participants (estimated)

Study arms

  • Experimental
    13C-Glucose

    Other: 13C-Glucose

  • Experimental
    13C-Acetate

    Other: 13C-Acetate

  • Experimental
    13C-Lactate

    Other: 13C-Lactate

  • Experimental
    13C-Glutamine

    Other: 13C-Glutamine

  • Experimental
    13C-Fructose

    Other: 13C-Fructose

Interventions

  • Other13C-Glucose

    Patients in the 13C-glucose arm will receive an infusion of a 13C-glucose solution. In most cases, the glucose infusion will be administered for 2-3 hours prior to resection of the mass. During the surgical procedure, 2-4mL of blood will be obtained approximately every 30 minutes to monitor blood glucose and/or blood pH. The infusion will be stopped after resection.

  • Other13C-Acetate

    Patients in the 13C-acetate arm will receive an infusion of a 13C-acetate solution. In most cases, the acetate infusion will be administered for 2-3 hours prior to resection of the mass. During the surgical procedure, 2-4mL of blood will be obtained approximately every 30 minutes to monitor blood glucose and/or blood pH. The infusion will be stopped after resection.

  • Other13C-Lactate

    Patients in the 13C-lactate arm will receive an infusion of a 13C-lactate solution. In most cases, the lactate infusion will be administered for 2-3 hours prior to resection of the mass. During the surgical procedure, 2-4mL of blood will be obtained approximately every 30 minutes to monitor blood glucose and/or blood pH. The infusion will be stopped after resection.

  • Other13C-Glutamine

    Patients in the 13C-glutamine arm will receive an infusion of a 13C-glutamine solution. In most cases, the glutamine infusion will be administered for 2-3 hours prior to resection of the mass. During the surgical procedure, 2-4mL of blood will be obtained approximately every 30 minutes to monitor blood glucose and/or blood pH. The infusion will be stopped after resection.

  • Other13C-Fructose

    Patients in the 13C-fructose arm will receive an infusion of a 13C-fructose solution. In most cases, the fructose infusion will be administered for 2-3 hours prior to resection of the mass. During the surgical procedure, 2-4mL of blood will be obtained approximately every 30 minutes to monitor blood glucose and/or blood pH. The infusion will be stopped after resection.

05

What researchers measure

Primary outcomes

  1. Percent of 13C isotopologue distributions

    Tissue and blood samples will be analyzed for 13C isotopologue distributions (percent) in central carbon metabolites using mass spectrometry. This allows the Investigators to understand how different subtypes of kidney and urothelial cancers alter utilization of the 13C tracers.

    Time frame: 5 years

06

Study locations

1 of 1 sites recruiting
  • University of Texas Southwestern Medical Center
    Dallas, Texas 75390, United States
    Recruiting
07

Registry details

Key details

Study ID
NCT04623502
Lead sponsor
University of Texas Southwestern Medical Center
Collaborators
Howard Hughes Medical Institute, National Cancer Institute (NCI)
Responsible party
Vitaly Margulis (Principal Investigator, Professor of Urology, University of Texas Southwestern Medical Center) — Principal investigator
First posted
Nov 10, 2020
Start date
Sep 30, 2019
Primary completion
Apr 30, 2027 (estimated)
Completion
Sep 30, 2027 (estimated)
Last update
Jan 28, 2026

Study contacts

Vitaly Margulis, MD
Contact
vitaly.margulis@utsouthwestern.edu
214-648-0567
Ralph J DeBerardinis, MD, PhD
Contact
ralph.deberardinis@utsouthwestern.edu
214-648-2585
Vitaly Margulis, MD
principal investigator · University of Texas Southwestern Medical Center

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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