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RECRUITING NA

Development of a Quantifiable Ultrasound Biomarker for Hepatic Steatosis

NCT07270601 · View on ClinicalTrials.gov ↗

Study Summary

The research study is considering a non-invasive way to measure the percentage of fat in the liver using ultrasound. This could help detect early signs of a very common condition called metabolic dysfunction-associated steatotic liver disease (MASLD). Current tests, like MRI or biopsy, can be expensive or invasive. If successful, this ultrasound tool could become an easier and more accessible way to monitor liver health - especially for people with obesity, diabetes, high blood pressure, or high cholesterol.

Interventions

  • DEVICE Verasonics NXT Data Acquisition System
  • DEVICE Philips EPIQ Elite
  • DEVICE EchoSense FibroScan
  • DEVICE Philips 3T Ingenia Elition

Study Locations (1)

Washington

  • University of Washington — Seattle

Trial Details

FieldValue
Enrollment Target 110 participants
Start Date 2025-11-17
Est. Completion 2026-12-31
Phase NA

Sponsor

ContextVision AB

1 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT07270601

The ClinicalTrials.gov registry entry for NCT07270601 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 110 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is ContextVision AB, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with MASLD - Metabolic Dysfunction-Associated Steatotic Liver Disease appearing as the primary indexed condition, and to 4 interventions — of which Verasonics NXT Data Acquisition System is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT07270601 reports 1 study location spanning 1 distinct geographic area — top geographies include Washington. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT07270601 about?

NCT07270601 is a clinical study titled "Development of a Quantifiable Ultrasound Biomarker for Hepatic Steatosis". The research study is considering a non-invasive way to measure the percentage of fat in the liver using ultrasound. This could help detect early signs of a very common condition called metabolic dysfunction-associated steatotic liver disease (MASLD). Current tests, like MRI or biopsy, can be expens...

What is the current status of trial NCT07270601?

This trial is currently recruiting. It is a NA study. The enrollment target is 110 participants. The study started on 2025-11-17. Estimated completion is 2026-12-31.

What conditions does trial NCT07270601 study?

This clinical trial studies the following conditions: MASLD - Metabolic Dysfunction-Associated Steatotic Liver Disease, NAFLD - Non-Alcoholic Fatty Liver Disease. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT07270601?

The interventions under investigation include: Verasonics NXT Data Acquisition System (DEVICE), Philips EPIQ Elite (DEVICE), EchoSense FibroScan (DEVICE), Philips 3T Ingenia Elition (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT07270601?

This trial is sponsored by ContextVision AB, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT07270601 being conducted?

This trial has 1 study location across Washington. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial