Carcinoma, HepatocellularPhase 4TRACERNCT06084234
National Liver Cancer Screening Trial
A Phase 4 study testing GALAD and Liver Ultrasound with or without AFP in people with Carcinoma, Hepatocellular and Liver Cancer, run by University of Texas Southwestern Medical Center at 19 sites in United States.
Trial summary
The National Liver Cancer Screening Trial is an adaptive randomized phase IV Trial comparing ultrasound-based versus biomarker-based screening in 5500 patients with cirrhosis from any etiology or patients with chronic hepatitis B infection. Read more about this study
- Who is it for?
- Ages 18 to 85 years
- Conditions the study is for
- Carcinoma, Hepatocellular, Liver Cancer, Liver Cirrhosis
- What is being tested?
- GALAD and Liver Ultrasound with or without AFP
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 5,500 participants
- Where
- 19 sitesUnited States
- Study dates
- 26 Dec 2023to 31 Dec 2034
- Phase
- Phase 4
- 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 18 to 85 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Patient must meet all of the following inclusion criteria:
- Adult patients ages 18-85 with cirrhosis from any etiology or with chronic hepatitis B with a PAGE-B score greater than 9 within 12 months of enrollment
- Patient is eligible for HCC surveillance according to treating physician or by the site investigator
- Able to provide informed consent
- Life expectancy >6 months (after consent) as determined by the treating provider or site investigator
Who cannot join
- Patient will be excluded for any of the following exclusion criteria:
- Child Pugh C cirrhosis
- History or clinical symptoms of hepatocellular carcinoma or cholangiocarcinoma
- History of solid nodule on baseline ultrasound (i.e., lesion 1cm or greater) within 9 months prior to consent without subsequent diagnostic CT/MRI demonstrating benign nature)
- AFP >20 ng/mL within 6 months prior to consent, in the absence of a contrast-enhanced CT or MRI within 6 months of AFP (before or after) level demonstrating lack of suspicious liver lesions
- Newly diagnosed LR-3 greater than or equal to 1 cm within 6 months prior to consent
Show all 20Show fewer
- History of LR-4, LR-5, or LR-M on multi-phase CT or contrast-enhanced MRI within 6 months prior to consent
- Presence of another active cancer besides non-melanomatous skin cancer or indolent cancer under active surveillance (e.g., prostate cancer or renal cell carcinoma) within the 2 years prior to consent
- Patient's provider is planning to use MRI- or CT- based surveillance moving forward
- History of a transjugular intrahepatic portosystemic shunt (TIPS)
- History of Fontan associated liver disease or cardiac cirrhosis
- History of solid organ transplantation
- Actively listed for liver transplantation
- Diagnosis of alcohol-associated hepatitis within 3 months prior to consent
- Documented current or continued signs and symptoms of acute Wilson disease (acute liver failure, acute neurological deficits, hemolysis)
- In patients with primary sclerosing cholangitis (PSC): Current active cholangitis within 90 days prior to consent
- Known or documented habitual non-adherence to previous research studies or medical procedures or unwillingness to adhere to protocol (e.g., unwilling to obtain consent or samples)
- In patients living with HIV: CD4+ T cell count less than 100 cells/mm3 within 60 days prior to consent
- Known pregnancy at consent
- Active warfarin use
Trial locations and contacts
19 sites in 1 country. Contact the study team or a site near you to ask about taking part.
19 sites in 1 country
United States19 sites, 18 recruiting
- Recruiting
University of Michigan
Ann Arbor, Michigan, 48109
Shay Robison, roshay@med.umich.edu
Neehar Parikh, MD, MS
- Recruiting
Massachusetts General Hospital
Boston, Massachusetts, 02114
Megan Michta, MMICHTA@mgh.harvard.edu
Irun Bhan, MD
- Recruiting
University of North Carolina
Chapel Hill, North Carolina, 27599
Andrew Moon, MD, 919-843-5936, Andrew.Moon@unchealth.unc.edu
Bhagyashree Behera, 919-843-5936, BB_Behera@med.unc.edu
- Recruiting
Northwestern University
Chicago, Illinois, 60611
Laura Kulik, MD, 312-694-1293, laura.kulik@nm.org
Kimberly Sipich, 312-694-1293, k-sipich@northwestern.edu
- Active, not recruiting
Case Western Reserve University
Cleveland, Ohio, 44106
- Recruiting
The Cleveland Clinic
Cleveland, Ohio, 44195
Taebin Son, 216-444-9508, Sont16@ccf.org
Shilpa Junna
- Recruiting
UT Southwestern Medical Center and Parkland Hospital
Dallas, Texas, 75390
Katharine McCallister, 214-645-1378, TRACER@UTSouthwestern.edu
Amit Singal, MD, MS
- Recruiting
Henry Ford Health System
Detroit, Michigan, 48202
Jessica Peruski, jperusk1@hfhs.org
Reena Salgia, MD
- Recruiting
Baylor College of Medicine
Houston, Texas, 77021
Emad Sorial, 713-798-7370, Emad.Sorial@bcm.edu
Sara.Fares@bcm.edu
- Recruiting
Indiana University
Indianapolis, Indiana, 46202
Sherri Cummins, shcummin@iu.edu
Naga Chalasani, MD
- Recruiting
University of Southern California
Los Angeles, California, 90089
Kali Zhou, MD
Kali Zhou, MD
- Recruiting
The Feinstein Institutes, Northwell Health, Inc.
Manhasset, New York, 11030
Dibnain Nanda, dnanda1@northwell.edu
Sanjaya Satapathy, MBBS, MS
- Recruiting
Hennepin Healthcare
Minneapolis, Minnesota, 55415
Jose Debes, MD, 9527379762, debes003@umn.edu
Daniel Akah, 9527379762, Dakah@bermancenter.org
- Recruiting
University of Minnesota
Minneapolis, Minnesota, 55455
Elizabeth Aby, MD, 612-625-8999, abyxx002@umn.edu
Erin Wesley, wesle091@umn.edu
- Recruiting
University of Pennsylvania
Philadelphia, Pennsylvania, 19104
Grace Kim, gracekim.lee@pennmedicine.upenn.edu
Jorge Marrero, MD,MS
- Recruiting
Stanford University
Redwood City, California, 94063
Paul Kwo, MD, 650-723-5135, pkwo@stanford.edu
Jennifer Smart, 650-721-8517, Jsmart2@stanford.edu
- Recruiting
Virginia Commonwealth University
Richmond, Virginia, 23219
Hannah Lee, MD, 804-828-4060, Hannah.Lee@vcuhealth.org
Hannah Cook, 804-628-9312, Hannah.Cook1@vcuhealth.org
- Recruiting
Kaiser Permanente
Roseville, California, 95661
Sreepriya Balasubramanian, MD, MPH, 916-474-6221, Sreepriya.Balasubramanian@kp.org
Quyen Chau, 415-833-3468, Quyen.X.Chau@kp.org
- Recruiting
University of California, San Francisco
San Francisco, California, 94117
Rae Davis, rayshawnda.davis@ucsf.edu
Neil Mehta, MD
About this study
The National Liver Cancer Screening Trial is an adaptive randomized phase IV Trial comparing ultrasound-based versus biomarker-based screening in 5500 patients with cirrhosis from any etiology or patients with chronic hepatitis B infection. Eligible patients will be randomized in a 1:1 fashion to Arm A using semi-annual ultrasound and AFP-based screening or Arm B using semi-annual screening using GALAD alone. Randomization will be stratified by sex, enrolling site, Child Pugh class (A vs. B), and HCC etiology (viral vs. non-viral). Patients will be recruited from 15 sites (mix of tertiary care and large community health systems) over a 3-year period, and the primary endpoint of the phase IV trial, reduction in late-stage HCC, will be assessed after 5.5 years.
Read the detailed description
The TRACER phase IV biomarker study is a randomized trial comparing ultrasound-based screening versus a biomarker-based strategy in patients with cirrhosis. In brief, 5500 patients with cirrhosis from any etiology would be randomized in a 1:1 fashion to Arm A offering semi-annual ultrasound +/- AFP-based screening or Arm B offering semi-annual biomarker-based screening. Randomization will be stratified by site, Child Pugh class (A vs. B), liver disease etiology (viral, non-viral, and non-cirrhotic HBV infection) and sex. Patients will be recruited from 15 sites (mix of tertiary care and large community health systems) over a 3-year period, and reduction in the proportion of late-stage HCC, will be assessed at the end of Year 5.5. If the results are promising, study team will continue extended follow-up and compare the incidence of late-stage HCC between the two arms at Year 8 and reduction in HCC mortality during long term follow up.
Study team will include adult patients, age ≥ 18 years, with Child Pugh class A or B cirrhosis of any etiology or non-cirrhotic chronic hepatitis B virus infection with PAGE-B score >9. Study team will exclude patients post liver transplantation, patients with Child Pugh C cirrhosis, patients with significant comorbidity and limited life expectancy, and those with history of other malignancy, except non-melanoma skin cancer or indolent tumors, within 3 years prior to enrollment given lack of screening recommendations in those patient populations. Study team will also exclude patients with suspicious liver masses at baseline as well as those with a solid lesion ≥1 cm on ultrasound or AFP ≥20 ng/mL without diagnostic evaluation to exclude HCC. Study team will also exclude patients in whom the provider plans to follow the patient with CT or MRI-based surveillance. GALAD is not recommended in patients with pregnancy or active warfarin use given known impact on biomarker performance, so these patients will be excluded.
At enrollment, study team will record patient demographics and clinical characteristics using a combination of electronic medical records and patient questionnaires. Patients will then be offered semi-annual surveillance as defined by their study arm: ultrasound and AFP for patients in Arm A and the biomarker, GALAD, for patients in Arm B. Repeat surveillance tests will be offered every six months (per assigned arm) for patients with normal surveillance results. Diagnostic evaluation with multi-phasic CT or contrast-enhanced MRI will be recommended for any patients with abnormal screening results. Patients with normal diagnostic testing (i.e., false positive result) will be recommended to return to their assigned surveillance arm. Standardized criteria from the AASLD and LI-RADS will be used to define incident HCC. Study team will use a set of validated surveys (e.g., Psychological Consequences Questionnaire, Decision Regret scale, FACIT-COST) to measure secondary outcomes of interest including psychological and financial harms.
- Conditions
- Carcinoma, Hepatocellular, Liver Cancer, Liver Cirrhosis, Hepatitis B
- Being tested
- GALAD, Liver Ultrasound with or without AFP
- Keywords
- Hepatocellular carcinoma surveillance, GALAD, Alpha Fetoprotein
- Medical subject headings
- Carcinoma, Hepatocellular, Liver Neoplasms, Liver Cirrhosis, Hepatitis B
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
GALADDiagnostic test
GALAD is a 3 biomarker panel incorporating AFP, AFP-L3% and DCP (all FDA approved), with patient age and sex.
Liver Ultrasound with or without AFPDiagnostic test
This intervention consists of current standard of care ultrasound based surveillance with or without alpha-fetoprotein measurement.
| Study group | Role | What they receive |
|---|---|---|
| Arm A: Semi-annual surveillance using liver ultrasound +/- alpha-fetoprotein | Active comparator | Participants in this arm will undergo current standard of care surveillance procedures i.e. liver ultrasound with or without alpha fetoprotein (AFP) measurement. Receives: Diagnostic Test: Liver Ultrasound with or without AFP |
| Arm B: Semi-annual surveillance using GALAD | Experimental | For participants in this arm, study team will order GALAD measurement every 6 months +/- 3 months. Receives: Diagnostic Test: GALAD |
What is being measured
The primary outcome is the main question the study is designed to answer.
Proportion of HCC detected at late stage
Proportion of HCC detected at a late stage, defined as HCC beyond Milan Criteria (one tumor less than or equal to 5 cm or 2-3 tumors each less than or equal to 3 cm, in the absence of vascular invasion or extra-hepatic metastases)
Measured: 5.5 years
Secondary outcomes (7)
HCC Screening utilization
Defined as proportion time covered by screening; each completed screening test (US +/- AFP or GALAD) will provide up to six months of coverage (numerator) divided by the total follow-up for each patient.
Measured: 5.5 years
Proportion of HCC detected at a late-stage (defined based on BCLC stage)
Defined as HCC beyond BCLC stage A (single tumor of any size without vascular invasion or extrahepatic spread; or 2-3 tumors equal to or less than 3 cm each, without vascular invasion or extrahepatic spread)
Measured: 5.5 years
Incidence of late-stage HCC
Defined as incidence of HCC (extended follow-up) beyond Milan Criteria or BCLC stage A
Measured: 8 years
Proportion of HCC cases that receive Curative therapy
Defined as count of participants in receipt of liver transplantation, surgical resection, local ablative therapy, or radiation segmentectomy
Measured: 5.5 years
Number of participants who encountered screening related physical harm
Physical harms will be defined as count of participants in receipt of diagnostic imaging for false positive or indeterminate results.
Measured: 5.5 years
Number of participants who encountered screening related financial harm
Financial harms will be defined by direct costs (charges for all screening and diagnostic testing and co-pays) and indirect costs (e.g., travel and lost wages)
Measured: 5.5 years
Number of participants who encountered screening related Psychological harm
Count of participants who encountered Psychological harms that includes cancer-specific worry and decisional regret.
Measured: 5.5 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted16 Oct 2023
- Study start26 Dec 2023
- Primary completion31 Dec 2029 (estimated)
- Study completion31 Dec 2034 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Carcinoma, HepatocellularStudies of the same condition, open and under way.
- More trials run by University of Texas Southwestern Medical CenterThe 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 4
- Primary purpose
- Screening
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- This is a randomized open-label study comparing US ± AFP vs. GALAD-based surveillance every 6 (± 3-month window) months starting at randomization.
- Masking
- None (open label)
- Enrolment
- 5,500 participants (estimated)
Sponsor and investigators
- Lead sponsor
- University of Texas Southwestern Medical Center
- Sponsor type
- University, hospital or other
- Collaborators
- National Cancer Institute (NCI), University of Pennsylvania, University of Michigan, Dana-Farber Cancer Institute, Baylor College of Medicine, Fred Hutchinson Cancer Center, The Cleveland Clinic
- Responsible party
- Principal investigator, Amit Singal, University of Texas Southwestern Medical Center
- Investigators
- Amit Singal, MD, MS, Principal investigator, University of Texas Southwestern Medical Center
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06084234
- Sponsor's protocol ID
- TRACER
- Other IDs
- 2U24CA086368-22
- Acronym
- TRACER
- Status last verified
- Sep 2026
- First submitted
- 10 Oct 2023
- Last updated
- 25 Sep 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- Yes
- Individual data sharing
- No
Publications
Singal AG, Parikh ND, Kanwal F, Marrero JA, Deodhar S, Page-Lester S, Lopez C, Feng Z, Tayob N. National Liver Cancer Screening Trial (TRACER) study protocol. Hepatol Commun. 2024 Nov 4;8(11):e0565. doi: 10.1097/HC9.0000000000000565. eCollection 2024 Nov 1.
PubMed 39495136
Study at a glance
From the registry record, last updated by the sponsor on 25 Sep 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- National Liver Cancer Screening Trial
- ClinicalTrials.gov ID
- NCT06084234
- Acronym / sponsor ID
- TRACER / TRACER
- Conditions
- Carcinoma, Hepatocellular, Liver Cancer, Liver Cirrhosis, Hepatitis B
- Keywords
- Hepatocellular carcinoma surveillance, GALAD, Alpha Fetoprotein
- Phase
- Phase 4
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 5,500 participants (estimated)
- Lead sponsor
- University of Texas Southwestern Medical CenterUniversity, hospital or other
- Collaborators
- National Cancer Institute (NCI), University of Pennsylvania, University of Michigan, Dana-Farber Cancer Institute, Baylor College of Medicine, Fred Hutchinson Cancer Center, The Cleveland Clinic
- Study start
- 26 Dec 2023 (actual)
- Primary completion
- 31 Dec 2029 (estimated)
- Study completion
- 31 Dec 2034 (estimated)
- First posted
- 16 Oct 2023 (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.
The National Liver Cancer Screening Trial is an adaptive randomized phase IV Trial comparing ultrasound-based versus biomarker-based screening in 5500 patients with cirrhosis from any etiology or patients with chronic hepatitis B infection. Eligible patients will be randomized in a 1:1 fashion to Arm A using semi-annual ultrasound and AFP-based screening or Arm B using semi-annual screening using GALAD alone. Randomization will be stratified by sex, enrolling site, Child Pugh class (A vs. B), and HCC etiology (viral vs. non-viral). Patients will be recruited from 15 sites (mix of tertiary care and large community health systems) over a 3-year period, and the primary endpoint of the phase IV trial, reduction in late-stage HCC, will be assessed after 5.5 years.
Detailed description
The TRACER phase IV biomarker study is a randomized trial comparing ultrasound-based screening versus a biomarker-based strategy in patients with cirrhosis. In brief, 5500 patients with cirrhosis from any etiology would be randomized in a 1:1 fashion to Arm A offering semi-annual ultrasound +/- AFP-based screening or Arm B offering semi-annual biomarker-based screening. Randomization will be stratified by site, Child Pugh class (A vs. B), liver disease etiology (viral, non-viral, and non-cirrhotic HBV infection) and sex. Patients will be recruited from 15 sites (mix of tertiary care and large community health systems) over a 3-year period, and reduction in the proportion of late-stage HCC, will be assessed at the end of Year 5.5. If the results are promising, study team will continue extended follow-up and compare the incidence of late-stage HCC between the two arms at Year 8 and reduction in HCC mortality during long term follow up.
Study team will include adult patients, age ≥ 18 years, with Child Pugh class A or B cirrhosis of any etiology or non-cirrhotic chronic hepatitis B virus infection with PAGE-B score >9. Study team will exclude patients post liver transplantation, patients with Child Pugh C cirrhosis, patients with significant comorbidity and limited life expectancy, and those with history of other malignancy, except non-melanoma skin cancer or indolent tumors, within 3 years prior to enrollment given lack of screening recommendations in those patient populations. Study team will also exclude patients with suspicious liver masses at baseline as well as those with a solid lesion ≥1 cm on ultrasound or AFP ≥20 ng/mL without diagnostic evaluation to exclude HCC. Study team will also exclude patients in whom the provider plans to follow the patient with CT or MRI-based surveillance. GALAD is not recommended in patients with pregnancy or active warfarin use given known impact on biomarker performance, so these patients will be excluded.
At enrollment, study team will record patient demographics and clinical characteristics using a combination of electronic medical records and patient questionnaires. Patients will then be offered semi-annual surveillance as defined by their study arm: ultrasound and AFP for patients in Arm A and the biomarker, GALAD, for patients in Arm B. Repeat surveillance tests will be offered every six months (per assigned arm) for patients with normal surveillance results. Diagnostic evaluation with multi-phasic CT or contrast-enhanced MRI will be recommended for any patients with abnormal screening results. Patients with normal diagnostic testing (i.e., false positive result) will be recommended to return to their assigned surveillance arm. Standardized criteria from the AASLD and LI-RADS will be used to define incident HCC. Study team will use a set of validated surveys (e.g., Psychological Consequences Questionnaire, Decision Regret scale, FACIT-COST) to measure secondary outcomes of interest including psychological and financial harms.
Study design
- Primary purpose
- Screening
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
- Model description
- This is a randomized open-label study comparing US ± AFP vs. GALAD-based surveillance every 6 (± 3-month window) months starting at randomization.
| Arm | Type | Receives |
|---|---|---|
| Arm A: Semi-annual surveillance using liver ultrasound +/- alpha-fetoprotein | Active comparator | Diagnostic Test: Liver Ultrasound with or without AFPParticipants in this arm will undergo current standard of care surveillance procedures i.e. liver ultrasound with or without alpha fetoprotein (AFP) measurement. |
| Arm B: Semi-annual surveillance using GALAD | Experimental | Diagnostic Test: GALADFor participants in this arm, study team will order GALAD measurement every 6 months +/- 3 months. |
Who may qualify
- Ages
- 18 to 85 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (5 listed)
- Adult patients ages 18-85 with cirrhosis from any etiology or with chronic hepatitis B with a PAGE-B score greater than 9 within 12 months of enrollment
- Patient is eligible for HCC surveillance according to treating physician or by the site investigator
- Able to provide informed consent
- Life expectancy >6 months (after consent) as determined by the treating provider or site investigator
Key exclusion criteria (20 listed)
- Child Pugh C cirrhosis
- History or clinical symptoms of hepatocellular carcinoma or cholangiocarcinoma
- History of solid nodule on baseline ultrasound (i.e., lesion 1cm or greater) within 9 months prior to consent without subsequent diagnostic CT/MRI demonstrating benign nature)
- AFP >20 ng/mL within 6 months prior to consent, in the absence of a contrast-enhanced CT or MRI within 6 months of AFP (before or after) level demonstrating lack of suspicious liver lesions
- Newly diagnosed LR-3 greater than or equal to 1 cm within 6 months prior to consent
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 |
|---|---|---|
| GALADGALAD is a 3 biomarker panel incorporating AFP, AFP-L3% and DCP (all FDA approved), with patient age and sex. | Diagnostic test | Arm B: Semi-annual surveillance using GALAD |
| Liver Ultrasound with or without AFPThis intervention consists of current standard of care ultrasound based surveillance with or without alpha-fetoprotein measurement. | Diagnostic test | Arm A: Semi-annual surveillance using liver ultrasound +/- alpha-fetoprotein |
Primary outcome
Proportion of HCC detected at late stage
Time frame: 5.5 years
Proportion of HCC detected at a late stage, defined as HCC beyond Milan Criteria (one tumor less than or equal to 5 cm or 2-3 tumors each less than or equal to 3 cm, in the absence of vascular invasion or extra-hepatic metastases)
7 secondary outcomes
HCC Screening utilization
Time frame: 5.5 years
Proportion of HCC detected at a late-stage (defined based on BCLC stage)
Time frame: 5.5 years
Incidence of late-stage HCC
Time frame: 8 years
Proportion of HCC cases that receive Curative therapy
Time frame: 5.5 years
Number of participants who encountered screening related physical harm
Time frame: 5.5 years
Number of participants who encountered screening related financial harm
Time frame: 5.5 years
Number of participants who encountered screening related Psychological harm
Time frame: 5.5 years
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 25 Sep 2026.
- Derived from this study: PubMed 39495136Singal AG, Parikh ND, Kanwal F, Marrero JA, Deodhar S, Page-Lester S, Lopez C, Feng Z, Tayob N. National Liver Cancer Screening Trial (TRACER) study protocol. Hepatol Commun. 2024 Nov 4;8(11):e0565. doi: 10.1097/HC9.0000000000000565. eCollection 2024 Nov 1.
- Individual participant dataSharing planned: No
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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.
Amit Singal, MD, MS principal investigator
University of Texas Southwestern Medical Center
19 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 4 study testing GALAD and Liver Ultrasound with or without AFP in people with Carcinoma, Hepatocellular and Liver Cancer, run by University of Texas Southwestern Medical Center at 19 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 5 inclusion and 20 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: looking for participants now, as of the sponsor's last update on 25 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 19 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.
What does this phase mean?
Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
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?
Contact Amit Singal, MD, MS (214-645-8821, Amit.Singal@UTSouthwestern.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Proportion of HCC detected at late stage (time frame: 5.5 years). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT06084234, which also lists 1 linked publication.
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 25 Sep 2026.