Imaging Changes in Liver Cancer with Nitroglycerin

This study is looking at how a medication called nitroglycerin, given directly into the artery (intra-arterially), affects blood flow in liver tumors (hepatocellular carcinoma or HCC). Researchers will use a special imaging technique called Parenchymal Blood Volume (PBV) imaging to see these changes. You might be able to join if you are an adult with newly diagnosed HCC that your doctors have decided is suitable for a standard treatment called trans-arterial chemoembolization (TACE). The main goal is to see if at least 30% of participants show an increase in blood flow to their tumor on the first day after receiving nitroglycerin. The current recruitment status is unclear.

Study design
This is a single-arm, open-label study involving about 50 participants. It is a first-in-human feasibility study.
What's involved
You would undergo PBV imaging before and after receiving intra-arterial nitroglycerin during your standard TACE treatment. You would then have follow-up appointments on days 3, 7, 30, and 90 after the procedure.
Compensation
Not stated in the trial record.
Follow-up
Participants will be followed for 90 days after the procedure.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07682454

Utilize Imaging to Assess Changes in Hepatocellular Carcinoma Perfusion as Potentiated by Intra-Arterial Nitroglycerin

Not Yet Recruiting
PHASE2Ages 18+InterventionalDiagnostic
University of California, San Francisco
~50 participants
Updated 2026-07-02 on ClinicalTrials.gov
What's tested:Parenchymal Blood Volume (PBV) ImagingNitroglycerinMedical Record Review

At a glance

Recruiting sites
0 of 2 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Proportion of Participants with >= 30% increase in Tumoral Blood Volume
Measured over Day 1
Hepatocellular Carcinoma (HCC)
Liver Cancer, Adult

NCT07682454

Where you'd take part

This study runs at 2 sites. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • University of California, San Francisco

    San Francisco, Californiastudy coordinator listed

  • Zuckerberg San Francisco General Hospital (ZSFG)

    San Francisco, Californiastudy coordinator listed

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

  • Christopher Brunson, MD · PRINCIPAL_INVESTIGATOR · University of California, San Francisco

Opens a ready-to-send draft in your own email app — review before sending.

  • Proportion of Participants with >= 30% increase in Tumoral Blood VolumeDay 1

    Proportion of participants who demonstrate an increase in tumoral blood volume of at least 30% following intra-arterial nitroglycerin administration compared with pre-nitroglycerin baseline along with Bonferroni-corrected confidence intervals will be reported.