Metabolic Dysfunction Associated Steatotic Liver DiseaseNCT06218589
Non-Invasive Diagnostic Tests for MASLD in Pediatric Population
A study testing Velacur, MRI and Blood sample collection for biomarkers in people with Metabolic Dysfunction Associated Steatotic Liver Disease and Non-Alcoholic Fatty Liver Disease (NAFLD), run by Emory University at 2 sites in United States.
Trial summary
This study aims to test the utility of Velacur ultrasound as a non-invasive, rapid, point of care diagnostic tool for detecting the presence and amount of hepatic steatosis in children and adolescents aged 2 - 20 years. Read more about this study
- Who is it for?
- Ages 2 to 20 years
- Conditions the study is for
- Metabolic Dysfunction Associated Steatotic Liver Disease, Non-Alcoholic Fatty Liver Disease (NAFLD)
- What is being tested?
- Velacur, MRI and Blood sample collection for biomarkers
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 200 participants
- Where
- 2 sitesUnited States
- Study dates
- 18 Jan 2024to Feb 2027
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 2 to 20 years
- All sexes
- No healthy volunteers
- Child, Adult
Who may be able to join
- Males and females age 2-20 years with suspicion of MASLD or presenting to liver clinic for evaluation of liver disease, including possible MASLD
- For participants choosing to do MRI they have to be able to undergo MRI without sedation
- Written/verbal informed consent from parent or legal guardian
- Written/verbal informed assent from the child when indicated by age
Who cannot join
- Ascites
- Pregnancy
- Failure to give consent or assent
- Have an implanted electronic device such as pacemaker, neurostimulator, or cochlear implant
Trial locations and contacts
2 sites in 1 country.
United States2 sites
Children's Healthcare of Atlanta (CHOA)
Atlanta, Georgia, 30322
Emory Children's Center
Atlanta, Georgia, 30322
About this study
Official title: Non-Invasive Diagnostic Tests for MASLD in Pediatric Population at an Outpatient Clinic: Velacur and Blood-based Novel Tests
This study aims to test the utility of Velacur ultrasound as a non-invasive, rapid, point of care diagnostic tool for detecting the presence and amount of hepatic steatosis in children and adolescents aged 2 - 20 years.
Read the detailed description
Non-Alcoholic Fatty Liver Disease (NAFLD) is currently the leading cause of liver disease in children. The name of NAFLD recently changed to metabolic dysfunction associated steatotic liver disease (MASLD). The definition of MASLD is the presence of steatosis in the liver and a metabolic abnormality, in the setting of other liver steatotic liver diseases having been ruled out. Due to its association with obesity and diabetes, MASLD prevalence is rising worldwide following the upward trends of these diseases. Among the United States pediatric population, the prevalence of NAFLD has been measured at around 11% and it varies widely among races. MASLD is likely very similar in numbers. Because of the natural history of the disease, MASLD patients are at risk of developing cardiovascular complications and hepatocellular carcinoma, raising the issue of diagnosing and treating promptly with the most accurate approaches.
Liver biopsy is the gold standard for assessing inflammation and fibrosis in metabolic dysfunction associated steatotic liver disease. This test is highly sensitive and specific, however some weaknesses exist. Liver biopsy uses a small sample size which can misrepresent the overall health/disease of the organ and there can be interpretation variability within the pathologists assessing the histology. Liver biopsy is also an invasive test, making it less desirable due to the potential of complications and cost. Due to these and despite being the most exact test, its invasive nature and its high price, make it not widely used.
There are several clinical needs, including a better way to rapidly diagnose MASLD in the outpatient clinic setting and to measure the severity of MASLD in patients already diagnosed. The first need, to diagnose MASLD requires demonstrating the presence of steatosis through imaging and sending some standard labs to rule out other conditions and assess metabolic features. The second need focuses primarily on fibrosis assessment, because the amount of fibrosis is the most closely associated with long term outcomes. While inflammation quantity is also important for staging MASLD, inflammation tends to rise and fall with changes in lifestyle and presents a less durable finding. Currently, in pediatrics the level of inflammatory injury is reasonably well represented by change in alanine transaminase (ALT). Thus, validating it is not a primary or secondary objective in this proposal.
The most accurate non-invasive imagining diagnostic test for hepatic steatosis in MASLD is Magnetic Resonance Imagining (MRI) and Magnetic Resonance Spectroscopy (MRS). Specifically, the MRI with Proton Density Fat Fraction (PDFF), has shown to have the best results at diagnosing liver steatosis since it is able to map for fat to the whole liver. Accurate fibrosis assessments have been accomplished with the use of Magnetic Resonance Elastography (MRE) and possess an advantage over ultrasound fibrosis measurements because it is independent of abdominal fat. In spite of that, this imaging is not widely available, and it is still highly priced making it less available.
There are a wide variety of ultrasound based tests measuring liver steatosis and it is an inexpensive alternative to diagnose and follow-up patients. Ultrasound is used in conjunction with scores to measure steatosis according to liver echogenicity and visibility of the surrounding organs. Nonetheless, the sensitivity to finding disease decreases for mild cases and only improves when patients have more than 20% hepatocytes that are fatty. Controlled Attenuation Parameter (CAP) in FibroScan machines has been used to address this issue by measuring the ultrasound attenuation and propagation speed of a shear wave delivered by an ultrasound probe (transient elastography, TE). Even though the CAP and TE provide better results, it still has its downfalls in being accurate when the patient is obese and not being extensively accessible.
Velacur is a liver ultrasound that measures hepatic fat and fibrosis through the propagation of a continuously, externally conducted shear wave. Velacur will measure hepatic steatosis and fibrosis through the measures of ultrasound attenuation and the propagation of a shear wave through the liver to measure its stiffness but will perform the stiffness reading using a continuous, externally conducted wave. This technology is thought to provide a better liver volume sample, giving a better reading in obese patients and the software gives live data for easy and fast patient follow-up, making it easy to use from Medical Assistants to Physicians.
There is a need to validate new non-invasive tests to find accurate diagnostic and liver disease staging tools that are simple to use, with easy access and affordable. Due to the small size of the Velacur device and similarity to other technologies available, and the opportunity of collecting blood biomarkers, the investigators want to study the possibility of using both technologies in an outpatient setting to screen and follow up pediatric population with MASLD in Atlanta, Georgia, USA. The investigators will complete a Velacur exam and/or collect blood biomarkers on patients recruited into the study. Statistical analysis will be performed comparing Velacur with the current gold standards of MRI and liver biopsy.
- Conditions
- Metabolic Dysfunction Associated Steatotic Liver Disease, Non-Alcoholic Fatty Liver Disease (NAFLD)
- Being tested
- Velacur, MRI, Blood sample collection for biomarkers, Liver biopsy
- Keywords
- Pediatrics
- Medical subject headings
- Non-alcoholic Fatty Liver Disease
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
VelacurDiagnostic test
Velacur is a liver ultrasound that measures hepatic fat and fibrosis through the propagation of a continuously, externally conducted shear wave. An enrolled participant may choose to do the ultrasound at the time of a clinic visit, or research visit or a scheduled radiology visit according to manufacturer's instructions by trained study staff. Fibrosis and steatosis measures will be collected from all scans.
MRIDiagnostic test
Participants who have not had an MRI within the past two years will be offered a research MRI (no contrast or sedation will be used) to measure hepatic fat and hepatic stiffness (if required). Participants who have had an MRI or liver biopsy in the past two years will use historical data comparison data. MRI data will include the PDFF hepatic fat, any assessment of fibrosis and notes of other abnormalities.
Blood sample collection for biomarkersDiagnostic test
Biomarkers are metabolic thumbprints of how the body is behaving to different health or disease processes, some of the biomarkers can be studied from plasma or serum combined with other demographics. A lipid profile and comprehensive metabolic panel (CMP), if not obtained clinically within 4 weeks, will be collected as a standard of care.
Liver biopsyDiagnostic test
Liver biopsy data will be collected only if liver biopsy is done clinically when available and scored using the Nonalcoholic Steatohepatitis Clinical Research Network (NASH CRN) approach.
| Study group | Role | What they receive |
|---|---|---|
| Velacur Ultrasound | Experimental | Patients 2 to 20 years of age with suspicion of MASLD or presenting to liver clinic for evaluation of liver disease, including possible MASLD receiving a Velacur ultrasound. Receives: Diagnostic Test: Velacur; Diagnostic Test: MRI; Diagnostic Test: Blood sample collection for biomarkers; Diagnostic Test: Liver biopsy |
What is being measured
The primary outcome is the main question the study is designed to answer.
Sensitivity of Detecting MASLD
The performance of Velacur is assessed as the percentage of correctly identified cases of MASLD (true positives) detected by Velacur imaging. The presence of MASLD will be compared with the determinations from MRI and liver biopsy, the current gold standards.
Measured: Day 1 (day of liver ultrasound)
Specificity of Detecting MASLD
The performance of Velacur is assessed as the percentage of correctly identified lack of MASLD (true negatives) detected by Velacur imaging. The presence of MASLD will be compared with the determinations from MRI and liver biopsy, the current gold standards.
Measured: Day 1 (day of liver ultrasound)
Positive Predictive Value (PPV)
The Positive Predictive Value (PPV) is the ratio of participants who are truly positive for MASLD divided by the number of participants who test positive for MASLD (true positives and false positives).
Measured: Day 1 (day of liver ultrasound)
Negative Predictive Values (NPV)
The Negative Predictive Value (NPV) is the ratio of participants who are truly negative for MASLD divided by the number of participants who test negative for MASLD (true negatives and false negatives).
Measured: Day 1 (day of liver ultrasound)
Area Under the Receiver Operating Curve (ROC)
The area under the receiver operating characteristic curve is used to assess the diagnostic ability of Velacur and MRI in this specific cohort. The area under the ROC ranges from 0 to 1, where 0 indicates that all predictions were incorrect and 1 means that all predictions were correct.
Measured: Day 1 (day of liver ultrasound)
Threshold of Detection Assessed by Youden Index
Thresholds for Velacur to detect MASLD vs non-MASLD (using MRI as the gold standard) will be calculated using the Youden index, maximizing the difference between true positive rate and false positive rate. The Youden Index ranges from 0 to 1 where 1 indicates that there were no false positives or false negatives (the test is perfect) and 0 means that the test is not an effective way to predict the MASLD.
Measured: Day 1 (day of liver ultrasound)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted23 Jan 2024
- Study start18 Jan 2024
- Primary completionFeb 2027 (estimated)
- Study completionFeb 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Metabolic Dysfunction Associated Steatotic Liver DiseaseStudies of the same condition, open and under way.
- More trials run by Emory UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Diagnosis
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 200 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Emory University
- Sponsor type
- University, hospital or other
- Collaborators
- Sonic Incytes, The Obesity Society
- Responsible party
- Principal investigator, Miriam Vos, Emory University
- Investigators
- Miriam Vos, MD, Principal investigator, Emory University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06218589
- Sponsor's protocol ID
- STUDY00006624
- Other IDs
- 2025P010537
- Status last verified
- Apr 2026
- First submitted
- 12 Jan 2024
- Last updated
- 8 Apr 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- Yes
- Individual data sharing
- Yes: De-identified participant data will be available for sharing with other researchers including anthropometrics, demographics, laboratory results.
Study at a glance
From the registry record, last updated by the sponsor on 8 Apr 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Non-Invasive Diagnostic Tests for MASLD in Pediatric Population at an Outpatient Clinic: Velacur and Blood-based Novel Tests
- ClinicalTrials.gov ID
- NCT06218589
- Acronym / sponsor ID
- STUDY00006624
- Conditions
- Metabolic Dysfunction Associated Steatotic Liver Disease, Non-Alcoholic Fatty Liver Disease (NAFLD)
- Keywords
- Pediatrics
- Study type
- Interventional
- Recruitment status
- Active, not recruiting
- Enrolment
- 200 participants (estimated)
- Lead sponsor
- Emory UniversityUniversity, hospital or other
- Collaborators
- Sonic Incytes, The Obesity Society
- Study start
- 18 Jan 2024 (actual)
- Primary completion
- Feb 2027 (estimated)
- Study completion
- Feb 2027 (estimated)
- First posted
- 23 Jan 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This study aims to test the utility of Velacur ultrasound as a non-invasive, rapid, point of care diagnostic tool for detecting the presence and amount of hepatic steatosis in children and adolescents aged 2 - 20 years.
Detailed description
Non-Alcoholic Fatty Liver Disease (NAFLD) is currently the leading cause of liver disease in children. The name of NAFLD recently changed to metabolic dysfunction associated steatotic liver disease (MASLD). The definition of MASLD is the presence of steatosis in the liver and a metabolic abnormality, in the setting of other liver steatotic liver diseases having been ruled out. Due to its association with obesity and diabetes, MASLD prevalence is rising worldwide following the upward trends of these diseases. Among the United States pediatric population, the prevalence of NAFLD has been measured at around 11% and it varies widely among races. MASLD is likely very similar in numbers. Because of the natural history of the disease, MASLD patients are at risk of developing cardiovascular complications and hepatocellular carcinoma, raising the issue of diagnosing and treating promptly with the most accurate approaches.
Liver biopsy is the gold standard for assessing inflammation and fibrosis in metabolic dysfunction associated steatotic liver disease. This test is highly sensitive and specific, however some weaknesses exist. Liver biopsy uses a small sample size which can misrepresent the overall health/disease of the organ and there can be interpretation variability within the pathologists assessing the histology. Liver biopsy is also an invasive test, making it less desirable due to the potential of complications and cost. Due to these and despite being the most exact test, its invasive nature and its high price, make it not widely used.
There are several clinical needs, including a better way to rapidly diagnose MASLD in the outpatient clinic setting and to measure the severity of MASLD in patients already diagnosed. The first need, to diagnose MASLD requires demonstrating the presence of steatosis through imaging and sending some standard labs to rule out other conditions and assess metabolic features. The second need focuses primarily on fibrosis assessment, because the amount of fibrosis is the most closely associated with long term outcomes. While inflammation quantity is also important for staging MASLD, inflammation tends to rise and fall with changes in lifestyle and presents a less durable finding. Currently, in pediatrics the level of inflammatory injury is reasonably well represented by change in alanine transaminase (ALT). Thus, validating it is not a primary or secondary objective in this proposal.
The most accurate non-invasive imagining diagnostic test for hepatic steatosis in MASLD is Magnetic Resonance Imagining (MRI) and Magnetic Resonance Spectroscopy (MRS). Specifically, the MRI with Proton Density Fat Fraction (PDFF), has shown to have the best results at diagnosing liver steatosis since it is able to map for fat to the whole liver. Accurate fibrosis assessments have been accomplished with the use of Magnetic Resonance Elastography (MRE) and possess an advantage over ultrasound fibrosis measurements because it is independent of abdominal fat. In spite of that, this imaging is not widely available, and it is still highly priced making it less available.
There are a wide variety of ultrasound based tests measuring liver steatosis and it is an inexpensive alternative to diagnose and follow-up patients. Ultrasound is used in conjunction with scores to measure steatosis according to liver echogenicity and visibility of the surrounding organs. Nonetheless, the sensitivity to finding disease decreases for mild cases and only improves when patients have more than 20% hepatocytes that are fatty. Controlled Attenuation Parameter (CAP) in FibroScan machines has been used to address this issue by measuring the ultrasound attenuation and propagation speed of a shear wave delivered by an ultrasound probe (transient elastography, TE). Even though the CAP and TE provide better results, it still has its downfalls in being accurate when the patient is obese and not being extensively accessible.
Velacur is a liver ultrasound that measures hepatic fat and fibrosis through the propagation of a continuously, externally conducted shear wave. Velacur will measure hepatic steatosis and fibrosis through the measures of ultrasound attenuation and the propagation of a shear wave through the liver to measure its stiffness but will perform the stiffness reading using a continuous, externally conducted wave. This technology is thought to provide a better liver volume sample, giving a better reading in obese patients and the software gives live data for easy and fast patient follow-up, making it easy to use from Medical Assistants to Physicians.
There is a need to validate new non-invasive tests to find accurate diagnostic and liver disease staging tools that are simple to use, with easy access and affordable. Due to the small size of the Velacur device and similarity to other technologies available, and the opportunity of collecting blood biomarkers, the investigators want to study the possibility of using both technologies in an outpatient setting to screen and follow up pediatric population with MASLD in Atlanta, Georgia, USA. The investigators will complete a Velacur exam and/or collect blood biomarkers on patients recruited into the study. Statistical analysis will be performed comparing Velacur with the current gold standards of MRI and liver biopsy.
Study design
- Primary purpose
- Diagnosis
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Velacur Ultrasound | Experimental | Diagnostic Test: Velacur, Diagnostic Test: MRI, Diagnostic Test: Blood sample collection for biomarkers, Diagnostic Test: Liver biopsyPatients 2 to 20 years of age with suspicion of MASLD or presenting to liver clinic for evaluation of liver disease, including possible MASLD receiving a Velacur ultrasound. |
Who may qualify
- Ages
- 2 to 20 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult
Key inclusion criteria (4 listed)
- Males and females age 2-20 years with suspicion of MASLD or presenting to liver clinic for evaluation of liver disease, including possible MASLD
- For participants choosing to do MRI they have to be able to undergo MRI without sedation
- Written/verbal informed consent from parent or legal guardian
- Written/verbal informed assent from the child when indicated by age
Key exclusion criteria (4 listed)
- Ascites
- Pregnancy
- Failure to give consent or assent
- Have an implanted electronic device such as pacemaker, neurostimulator, or cochlear implant
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| VelacurVelacur is a liver ultrasound that measures hepatic fat and fibrosis through the propagation of a continuously, externally conducted shear wave. An enrolled participant may choose to do the ultrasound at the time of a clinic visit, or research visit or a scheduled radiology visit according to manufacturer's instructions by trained study staff. Fibrosis and steatosis measures will be collected from all scans. | Diagnostic test | Velacur Ultrasound |
| MRIParticipants who have not had an MRI within the past two years will be offered a research MRI (no contrast or sedation will be used) to measure hepatic fat and hepatic stiffness (if required). Participants who have had an MRI or liver biopsy in the past two years will use historical data comparison data. MRI data will include the PDFF hepatic fat, any assessment of fibrosis and notes of other abnormalities. | Diagnostic test | Velacur Ultrasound |
| Blood sample collection for biomarkersBiomarkers are metabolic thumbprints of how the body is behaving to different health or disease processes, some of the biomarkers can be studied from plasma or serum combined with other demographics. A lipid profile and comprehensive metabolic panel (CMP), if not obtained clinically within 4 weeks, will be collected as a standard of care. | Diagnostic test | Velacur Ultrasound |
| Liver biopsyLiver biopsy data will be collected only if liver biopsy is done clinically when available and scored using the Nonalcoholic Steatohepatitis Clinical Research Network (NASH CRN) approach. | Diagnostic test | Velacur Ultrasound |
Primary outcome
Sensitivity of Detecting MASLD
Time frame: Day 1 (day of liver ultrasound)
The performance of Velacur is assessed as the percentage of correctly identified cases of MASLD (true positives) detected by Velacur imaging. The presence of MASLD will be compared with the determinations from MRI and liver biopsy, the current gold standards.
Specificity of Detecting MASLD
Time frame: Day 1 (day of liver ultrasound)
The performance of Velacur is assessed as the percentage of correctly identified lack of MASLD (true negatives) detected by Velacur imaging. The presence of MASLD will be compared with the determinations from MRI and liver biopsy, the current gold standards.
Positive Predictive Value (PPV)
Time frame: Day 1 (day of liver ultrasound)
The Positive Predictive Value (PPV) is the ratio of participants who are truly positive for MASLD divided by the number of participants who test positive for MASLD (true positives and false positives).
Negative Predictive Values (NPV)
Time frame: Day 1 (day of liver ultrasound)
The Negative Predictive Value (NPV) is the ratio of participants who are truly negative for MASLD divided by the number of participants who test negative for MASLD (true negatives and false negatives).
Area Under the Receiver Operating Curve (ROC)
Time frame: Day 1 (day of liver ultrasound)
The area under the receiver operating characteristic curve is used to assess the diagnostic ability of Velacur and MRI in this specific cohort. The area under the ROC ranges from 0 to 1, where 0 indicates that all predictions were incorrect and 1 means that all predictions were correct.
Threshold of Detection Assessed by Youden Index
Time frame: Day 1 (day of liver ultrasound)
Thresholds for Velacur to detect MASLD vs non-MASLD (using MRI as the gold standard) will be calculated using the Youden index, maximizing the difference between true positive rate and false positive rate. The Youden Index ranges from 0 to 1 where 1 indicates that there were no false positives or false negatives (the test is perfect) and 0 means that the test is not an effective way to predict the MASLD.
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 8 Apr 2026.
- Individual participant dataSharing planned: Yes. De-identified participant data will be available for sharing with other researchers including anthropometrics, demographics, laboratory results.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Miriam Vos, MD principal investigator
Emory University
2 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Velacur, MRI and Blood sample collection for biomarkers in people with Metabolic Dysfunction Associated Steatotic Liver Disease and Non-Alcoholic Fatty Liver Disease (NAFLD), run by Emory University at 2 sites in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: under way, not looking for participants, as of the sponsor's last update on 8 Apr 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 2 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Sensitivity of Detecting MASLD (time frame: Day 1 (day of liver ultrasound)). The study lists 6 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 8 Apr 2026.